Canonical Allele Identifier: CA471495649
Gene: CYP17A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104596984T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837227T>C , CM000672.2:g.102837227T>C GRCh38
NC_000010.10:g.104596984T>C , CM000672.1:g.104596984T>C GRCh37
NC_000010.9:g.104586974T>C NCBI36
NG_007955.1:g.5307A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.135A>G MANE Select ENSP00000358903.3:p.Arg45=
ENST00000638190.1:c.135A>G ENSP00000492539.1:p.Arg45=
ENST00000638272.1:c.135A>G ENSP00000491508.1:p.Arg45=
ENST00000638971.1:c.135A>G ENSP00000492313.1:p.Arg45=
ENST00000639393.1:c.135A>G ENSP00000492651.1:p.Arg45=
ENST00000369887.3:c.135A>G ENSP00000358903.3:p.Arg45=
ENST00000489268.1:n.188A>G
NM_000102.3:c.135A>G NP_000093.1:p.Arg45=
NM_000102.4:c.135A>G MANE Select NP_000093.1:p.Arg45=
Search 100 bp 5'
Search 100 bp 3'