Canonical Allele Identifier: CA2610725929
Gene: CYP17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-102837485-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837485T>G , CM000672.2:g.102837485T>G GRCh38
NC_000010.10:g.104597242T>G , CM000672.1:g.104597242T>G GRCh37
NC_000010.9:g.104587232T>G NCBI36
NG_007955.1:g.5049A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-124A>C ENSP00000358903.3:n.-124A>C
NM_000102.3:c.-124A>C NP_000093.1:n.-124A>C
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