Linked Data
gnomAD v4:
1-1232699-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1232699G>C , CM000663.2:g.1232699G>C | GRCh38 |
| NC_000001.10:g.1168079G>C , CM000663.1:g.1168079G>C | GRCh37 |
| NC_000001.9:g.1157942G>C | NCBI36 |
| NG_030007.1:g.4369C>G | |
| NG_033265.1:g.5451G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379198.5:c.421G>C MANE Select | ENSP00000368496.2:p.Ala141Pro | |
| ENST00000379198.3:c.421G>C | ENSP00000368496.2:p.Ala141Pro | |
| NM_080605.3:c.421G>C | NP_542172.2:p.Ala141Pro | |
| NM_080605.4:c.421G>C MANE Select | NP_542172.2:p.Ala141Pro |