Canonical Allele Identifier: CA595636666
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs947279085
gnomAD v2: 10-104597243-G-C
gnomAD v3: 10-102837486-G-C
gnomAD v4: 10-102837486-G-C
MyVariant Identifiers: chr10:g.104597243G>C (hg19) chr10:g.102837486G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837486G>C , CM000672.2:g.102837486G>C GRCh38
NC_000010.10:g.104597243G>C , CM000672.1:g.104597243G>C GRCh37
NC_000010.9:g.104587233G>C NCBI36
NG_007955.1:g.5048C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-125C>G ENSP00000358903.3:n.-125C>G
NM_000102.3:c.-125C>G NP_000093.1:n.-125C>G
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