Canonical Allele Identifier: CA1932841528
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs1844181058

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837476G>C , CM000672.2:g.102837476G>C GRCh38
NC_000010.10:g.104597233G>C , CM000672.1:g.104597233G>C GRCh37
NC_000010.9:g.104587223G>C NCBI36
NG_007955.1:g.5058C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-115C>G ENSP00000358903.3:n.-115C>G
NM_000102.3:c.-115C>G NP_000093.1:n.-115C>G