Canonical Allele Identifier: CA1932841552
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837512C= , CM000672.2:g.102837512C= GRCh38
NC_000010.10:g.104597269C= , CM000672.1:g.104597269C= GRCh37
NC_000010.9:g.104587259C= NCBI36
NG_007955.1:g.5022G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-151G= ENSP00000358903.3:n.-151G=
NM_000102.3:c.-151G= NP_000093.1:n.-151G=