Canonical Allele Identifier: CA2610725948
Gene: CYP17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-102837505-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837505C>A , CM000672.2:g.102837505C>A GRCh38
NC_000010.10:g.104597262C>A , CM000672.1:g.104597262C>A GRCh37
NC_000010.9:g.104587252C>A NCBI36
NG_007955.1:g.5029G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-144G>T ENSP00000358903.3:n.-144G>T
NM_000102.3:c.-144G>T NP_000093.1:n.-144G>T
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