Canonical Allele Identifier: CA2610725944
Gene: CYP17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-102837500-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837500T>A , CM000672.2:g.102837500T>A GRCh38
NC_000010.10:g.104597257T>A , CM000672.1:g.104597257T>A GRCh37
NC_000010.9:g.104587247T>A NCBI36
NG_007955.1:g.5034A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-139A>T ENSP00000358903.3:n.-139A>T
NM_000102.3:c.-139A>T NP_000093.1:n.-139A>T
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