Linked Data
dbSNP Id:
rs151254980
ExAC:
19:18710600 C / G
gnomAD v2:
19-18710600-C-G
gnomAD v3:
19-18599790-C-G
gnomAD v4:
19-18599790-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18599790C>G , CM000681.2:g.18599790C>G | GRCh38 |
| NC_000019.9:g.18710600C>G , CM000681.1:g.18710600C>G | GRCh37 |
| NC_000019.8:g.18571600C>G | NCBI36 |
| NG_013370.1:g.12061G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684169.1:c.172G>C | ENSP00000506849.1:p.Ala58Pro | |
| ENST00000392386.8:c.172G>C MANE Select | ENSP00000376188.2:p.Ala58Pro | |
| ENST00000392386.7:c.172G>C | ENSP00000376188.2:p.Ala58Pro | |
| ENST00000593286.1:n.424G>C | ||
| NM_004750.4:c.172G>C | NP_004741.1:p.Ala58Pro | |
| XM_011528422.1:c.106G>C | XP_011526724.1:p.Ala36Pro | |
| XM_011528423.1:c.172G>C | XP_011526725.1:p.Ala58Pro | |
| XM_011528424.1:c.106G>C | XP_011526726.1:p.Ala36Pro | |
| XM_011528422.2:c.106G>C | XP_011526724.1:p.Ala36Pro | |
| XM_011528423.2:c.172G>C | XP_011526725.1:p.Ala58Pro | |
| XM_011528424.3:c.106G>C | XP_011526726.1:p.Ala36Pro | |
| NM_004750.5:c.172G>C MANE Select | NP_004741.1:p.Ala58Pro |