Canonical Allele Identifier: CA2610725909
Gene: CYP17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-102837445-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837445A>C , CM000672.2:g.102837445A>C GRCh38
NC_000010.10:g.104597202A>C , CM000672.1:g.104597202A>C GRCh37
NC_000010.9:g.104587192A>C NCBI36
NG_007955.1:g.5089T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000638190.1:c.-84T>G ENSP00000492539.1:n.-84T>G
ENST00000638971.1:c.-84T>G ENSP00000492313.1:n.-84T>G
ENST00000369887.3:c.-84T>G ENSP00000358903.3:n.-84T>G
NM_000102.3:c.-84T>G NP_000093.1:n.-84T>G
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