Canonical Allele Identifier: CA1932841555
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837521C= , CM000672.2:g.102837521C= GRCh38
NC_000010.10:g.104597278C= , CM000672.1:g.104597278C= GRCh37
NC_000010.9:g.104587268C= NCBI36
NG_007955.1:g.5013G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-160G= ENSP00000358903.3:n.-160G=
NM_000102.3:c.-160G= NP_000093.1:n.-160G=