Canonical Allele Identifier: CA1932841520
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs1844180879
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837461T>A , CM000672.2:g.102837461T>A GRCh38
NC_000010.10:g.104597218T>A , CM000672.1:g.104597218T>A GRCh37
NC_000010.9:g.104587208T>A NCBI36
NG_007955.1:g.5073A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000638190.1:c.-100A>T ENSP00000492539.1:n.-100A>T
ENST00000638971.1:c.-100A>T ENSP00000492313.1:n.-100A>T
ENST00000369887.3:c.-100A>T ENSP00000358903.3:n.-100A>T
NM_000102.3:c.-100A>T NP_000093.1:n.-100A>T
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