gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186535189G>C , CM000666.2:g.186535189G>C | GRCh38 |
| NC_000004.11:g.187456343G>C , CM000666.1:g.187456343G>C | GRCh37 |
| NC_000004.10:g.187693337G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703170.1:c.185-632C>G | ENSP00000515216.1:n.185-632C>G | |
| ENST00000307161.5:c.185-632C>G MANE Select | ENSP00000302811.5:n.185-632C>G | |
| ENST00000509111.2:c.147+19993C>G | ||
| NM_005958.3:c.185-632C>G | NP_005949.1:n.185-632C>G | |
| XM_011532002.1:c.-71-632C>G | XP_011530304.1:n.-71-632C>G | |
| XR_939589.1:n.1982-10455G>C | ||
| XR_939590.1:n.162-10455G>C | ||
| NM_005958.4:c.185-632C>G MANE Select | NP_005949.1:n.185-632C>G | |
| XM_011532002.3:c.-71-632C>G | XP_011530304.1:n.-71-632C>G | |
| XR_939589.2:n.1982-10455G>C | ||
| XR_939590.2:n.162-10455G>C |