Linked Data
dbSNP Id:
rs368572644
gnomAD v2:
10-104593747-G-C
gnomAD v3:
10-102833990-G-C
gnomAD v4:
10-102833990-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102833990G>C , CM000672.2:g.102833990G>C | GRCh38 |
| NC_000010.10:g.104593747G>C , CM000672.1:g.104593747G>C | GRCh37 |
| NC_000010.9:g.104583737G>C | NCBI36 |
| NG_007955.1:g.8544C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369884.4:n.152-187G>C | ||
| ENST00000369887.4:c.753+46C>G (CYP17A1) MANE Select | ENSP00000358903.3:n.753+46C>G | |
| ENST00000638190.1:c.666+795C>G (CYP17A1) | ENSP00000492539.1:n.666+795C>G | |
| ENST00000638272.1:c.298-782C>G (CYP17A1) | ENSP00000491508.1:n.298-782C>G | |
| ENST00000638971.1:c.667-782C>G (CYP17A1) | ENSP00000492313.1:n.667-782C>G | |
| ENST00000639393.1:c.753+46C>G (CYP17A1) | ENSP00000492651.1:n.753+46C>G | |
| ENST00000640633.1:n.515+46C>G (CYP17A1) | ||
| ENST00000369887.3:c.753+46C>G (CYP17A1) | ENSP00000358903.3:n.753+46C>G | |
| ENST00000489268.1:n.1715C>G (CYP17A1) | ||
| NM_000102.3:c.753+46C>G (CYP17A1) | NP_000093.1:n.753+46C>G | |
| XR_428804.1:n.206-187G>C (CYP17A1-AS1) | ||
| NM_000102.4:c.753+46C>G (CYP17A1) MANE Select | NP_000093.1:n.753+46C>G |