Canonical Allele Identifier: CA2610725900
Gene: CYP17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-102837432-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837432G>T , CM000672.2:g.102837432G>T GRCh38
NC_000010.10:g.104597189G>T , CM000672.1:g.104597189G>T GRCh37
NC_000010.9:g.104587179G>T NCBI36
NG_007955.1:g.5102C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000638190.1:c.-71C>A ENSP00000492539.1:n.-71C>A
ENST00000638971.1:c.-71C>A ENSP00000492313.1:n.-71C>A
ENST00000369887.3:c.-71C>A ENSP00000358903.3:n.-71C>A
NM_000102.3:c.-71C>A NP_000093.1:n.-71C>A
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