Canonical Allele Identifier: CA659060450
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs1377937962
gnomAD v4: 10-102836661-C-T
MyVariant Identifiers: chr10:g.104596418C>T (hg19) chr10:g.102836661C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102836661C>T , CM000672.2:g.102836661C>T GRCh38
NC_000010.10:g.104596418C>T , CM000672.1:g.104596418C>T GRCh37
NC_000010.9:g.104586408C>T NCBI36
NG_007955.1:g.5873G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.297+404G>A MANE Select ENSP00000358903.3:n.297+404G>A
ENST00000638190.1:c.297+404G>A ENSP00000492539.1:n.297+404G>A
ENST00000638272.1:c.297+404G>A ENSP00000491508.1:n.297+404G>A
ENST00000638971.1:c.297+404G>A ENSP00000492313.1:n.297+404G>A
ENST00000639393.1:c.297+404G>A ENSP00000492651.1:n.297+404G>A
ENST00000640633.1:n.59+53G>A
ENST00000369887.3:c.297+404G>A ENSP00000358903.3:n.297+404G>A
ENST00000489268.1:n.350+404G>A
NM_000102.3:c.297+404G>A NP_000093.1:n.297+404G>A
NM_000102.4:c.297+404G>A MANE Select NP_000093.1:n.297+404G>A
Search 100 bp 5'
Search 100 bp 3'