Canonical Allele Identifier: CA2610725908
Gene: CYP17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-102837443-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837443A>G , CM000672.2:g.102837443A>G GRCh38
NC_000010.10:g.104597200A>G , CM000672.1:g.104597200A>G GRCh37
NC_000010.9:g.104587190A>G NCBI36
NG_007955.1:g.5091T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000638190.1:c.-82T>C ENSP00000492539.1:n.-82T>C
ENST00000638971.1:c.-82T>C ENSP00000492313.1:n.-82T>C
ENST00000369887.3:c.-82T>C ENSP00000358903.3:n.-82T>C
NM_000102.3:c.-82T>C NP_000093.1:n.-82T>C
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