Canonical Allele Identifier: CA2610725941
Gene: CYP17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-102837498-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837498G>C , CM000672.2:g.102837498G>C GRCh38
NC_000010.10:g.104597255G>C , CM000672.1:g.104597255G>C GRCh37
NC_000010.9:g.104587245G>C NCBI36
NG_007955.1:g.5036C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-137C>G ENSP00000358903.3:n.-137C>G
NM_000102.3:c.-137C>G NP_000093.1:n.-137C>G
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