Linked Data
dbSNP Id:
rs778298833
gnomAD v2:
10-104591188-G-A
gnomAD v3:
10-102831431-G-A
gnomAD v4:
10-102831431-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102831431G>A , CM000672.2:g.102831431G>A | GRCh38 |
| NC_000010.10:g.104591188G>A , CM000672.1:g.104591188G>A | GRCh37 |
| NC_000010.9:g.104581178G>A | NCBI36 |
| NG_007955.1:g.11103C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369887.4:c.1243+77C>T (CYP17A1) MANE Select | ENSP00000358903.3:n.1243+77C>T | |
| ENST00000638190.1:c.940+77C>T (CYP17A1) | ENSP00000492539.1:n.940+77C>T | |
| ENST00000638272.1:c.787+77C>T (CYP17A1) | ENSP00000491508.1:n.787+77C>T | |
| ENST00000638971.1:c.1156+77C>T (CYP17A1) | ENSP00000492313.1:n.1156+77C>T | |
| ENST00000639393.1:c.1246+77C>T (CYP17A1) | ENSP00000492651.1:n.1246+77C>T | |
| ENST00000640633.1:n.1005+77C>T (CYP17A1) | ||
| ENST00000647664.1:c.*629-167G>A (WBP1L) | ENSP00000498131.1:n.*629-167G>A | |
| ENST00000369887.3:c.1243+77C>T (CYP17A1) | ENSP00000358903.3:n.1243+77C>T | |
| ENST00000469683.1:n.196+77C>T (CYP17A1) | ||
| NM_000102.3:c.1243+77C>T (CYP17A1) | NP_000093.1:n.1243+77C>T | |
| NM_000102.4:c.1243+77C>T (CYP17A1) MANE Select | NP_000093.1:n.1243+77C>T |