Canonical Allele Identifier: CA659061706
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs1428531623
gnomAD v3: 10-102837495-A-G
gnomAD v4: 10-102837495-A-G
MyVariant Identifiers: chr10:g.104597252A>G (hg19) chr10:g.102837495A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837495A>G , CM000672.2:g.102837495A>G GRCh38
NC_000010.10:g.104597252A>G , CM000672.1:g.104597252A>G GRCh37
NC_000010.9:g.104587242A>G NCBI36
NG_007955.1:g.5039T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-134T>C ENSP00000358903.3:n.-134T>C
NM_000102.3:c.-134T>C NP_000093.1:n.-134T>C
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