Canonical Allele Identifier: CA1932841536
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837489T= , CM000672.2:g.102837489T= GRCh38
NC_000010.10:g.104597246T= , CM000672.1:g.104597246T= GRCh37
NC_000010.9:g.104587236T= NCBI36
NG_007955.1:g.5045A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-128A= ENSP00000358903.3:n.-128A=
NM_000102.3:c.-128A= NP_000093.1:n.-128A=