Canonical Allele Identifier: CA5669678
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs756869744
ExAC: 10:104597169 G / T
gnomAD v2: 10-104597169-G-T
gnomAD v3: 10-102837412-G-T
gnomAD v4: 10-102837412-G-T
MyVariant Identifiers: chr10:g.104597169G>T (hg19) chr10:g.102837412G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837412G>T , CM000672.2:g.102837412G>T GRCh38
NC_000010.10:g.104597169G>T , CM000672.1:g.104597169G>T GRCh37
NC_000010.9:g.104587159G>T NCBI36
NG_007955.1:g.5122C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.-51C>A MANE Select ENSP00000358903.3:n.-51C>A
ENST00000638190.1:c.-51C>A ENSP00000492539.1:n.-51C>A
ENST00000638272.1:c.-51C>A ENSP00000491508.1:n.-51C>A
ENST00000638971.1:c.-51C>A ENSP00000492313.1:n.-51C>A
ENST00000639393.1:c.-51C>A ENSP00000492651.1:n.-51C>A
ENST00000369887.3:c.-51C>A ENSP00000358903.3:n.-51C>A
ENST00000489268.1:n.3C>A
NM_000102.3:c.-51C>A NP_000093.1:n.-51C>A
NM_000102.4:c.-51C>A MANE Select NP_000093.1:n.-51C>A
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