gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.9751095 (EAS)
Genomes Max Group AF
0.95317045 (EAS)
Exomes Max Group AF
0.97579467 (EAS)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10286566A>C , CM000665.2:g.10286566A>C | GRCh38 |
| NC_000003.11:g.10328250A>C , CM000665.1:g.10328250A>C | GRCh37 |
| NC_000003.10:g.10303250A>C | NCBI36 |
| NG_011560.1:g.11382T>G | |
| NG_033090.1:g.10615A>C | |
| NG_033090.2:g.10615A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000335542.13:c.334+138T>G (GHRL) MANE Select | ENSP00000335074.8:n.334+138T>G | |
| ENST00000287656.11:c.331+138T>G (GHRL) | ENSP00000287656.7:n.331+138T>G | |
| ENST00000335542.12:c.334+138T>G (GHRL) | ENSP00000335074.8:n.334+138T>G | |
| ENST00000422159.5:c.226-672T>G (GHRL) | ENSP00000405464.1:n.226-672T>G | |
| ENST00000429122.1:c.334+138T>G (GHRL) | ENSP00000414819.1:n.334+138T>G | |
| ENST00000430179.5:c.331+138T>G (GHRL) | ENSP00000399922.1:n.331+138T>G | |
| ENST00000437422.6:c.298+138T>G (GHRL) | ENSP00000416768.2:n.298+138T>G | |
| ENST00000439975.6:c.181+138T>G (GHRL) | ENSP00000403725.2:n.181+138T>G | |
| ENST00000446937.2:c.73-672T>G (GHRL) | ENSP00000394923.2:n.73-672T>G | |
| ENST00000449238.6:c.295+138T>G (GHRL) | ENSP00000388145.2:n.295+138T>G | |
| ENST00000457360.5:c.334+138T>G (GHRL) | ENSP00000391406.1:n.334+138T>G | |
| ENST00000475759.5:n.454+138T>G (GHRL) | ||
| ENST00000476283.1:n.646+138T>G (GHRL) | ||
| ENST00000481287.5:n.511+138T>G (GHRL) | ||
| ENST00000491589.5:n.425+138T>G (GHRL) | ||
| NM_001134941.2:c.331+138T>G (GHRL) | NP_001128413.1:n.331+138T>G | |
| NM_001134944.1:c.298+138T>G (GHRL) | NP_001128416.1:n.298+138T>G | |
| NM_001134945.1:c.295+138T>G (GHRL) | NP_001128417.1:n.295+138T>G | |
| NM_001134946.1:c.181+138T>G (GHRL) | NP_001128418.1:n.181+138T>G | |
| NM_001302821.1:c.334+138T>G (GHRL) | NP_001289750.1:n.334+138T>G | |
| NM_001302822.1:c.334+138T>G (GHRL) | NP_001289751.1:n.334+138T>G | |
| NM_001302823.1:c.331+138T>G (GHRL) | NP_001289752.1:n.331+138T>G | |
| NM_001302824.1:c.334+138T>G (GHRL) | NP_001289753.1:n.334+138T>G | |
| NM_001302825.1:c.334+138T>G (GHRL) | NP_001289754.1:n.334+138T>G | |
| NM_016362.4:c.334+138T>G (GHRL) | NP_057446.1:n.334+138T>G | |
| NR_004431.3:n.157+713A>C (GHRLOS) | ||
| NR_024144.2:n.240+713A>C (GHRLOS) | ||
| NR_024145.2:n.397+713A>C (GHRLOS) | ||
| NR_073566.1:n.336+713A>C (GHRLOS) | ||
| NR_073567.1:n.240+713A>C (GHRLOS) | ||
| NR_073568.1:n.240+713A>C (GHRLOS) | ||
| NR_126505.1:n.107-672T>G (GHRL) | ||
| XM_017006612.2:c.334+138T>G (GHRL) | XP_016862101.1:n.334+138T>G | |
| XM_017006613.2:c.331+138T>G (GHRL) | XP_016862102.1:n.331+138T>G | |
| XM_024453594.1:c.334+138T>G (GHRL) | XP_024309362.1:n.334+138T>G | |
| NM_001134941.3:c.331+138T>G (GHRL) | NP_001128413.1:n.331+138T>G | |
| NM_001134944.2:c.298+138T>G (GHRL) | NP_001128416.1:n.298+138T>G | |
| NM_001134945.2:c.295+138T>G (GHRL) | NP_001128417.1:n.295+138T>G | |
| NM_001134946.2:c.181+138T>G (GHRL) | NP_001128418.1:n.181+138T>G | |
| NM_001302821.2:c.334+138T>G (GHRL) | NP_001289750.1:n.334+138T>G | |
| NM_001302822.2:c.334+138T>G (GHRL) | NP_001289751.1:n.334+138T>G | |
| NM_001302823.2:c.331+138T>G (GHRL) | NP_001289752.1:n.331+138T>G | |
| NM_001302824.2:c.334+138T>G (GHRL) | NP_001289753.1:n.334+138T>G | |
| NM_001302825.2:c.334+138T>G (GHRL) | NP_001289754.1:n.334+138T>G | |
| NM_016362.5:c.334+138T>G (GHRL) MANE Select | NP_057446.1:n.334+138T>G | |
| NR_126505.2:n.107-672T>G (GHRL) |