Canonical Allele Identifier: CA5669651
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1154861
ClinVar RCV Id: RCV001496988
dbSNP Id: rs112892739
ExAC: 10:104597011 C / G
gnomAD v2: 10-104597011-C-G
gnomAD v4: 10-102837254-C-G
MyVariant Identifiers: chr10:g.104597011C>G (hg19) chr10:g.102837254C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837254C>G , CM000672.2:g.102837254C>G GRCh38
NC_000010.10:g.104597011C>G , CM000672.1:g.104597011C>G GRCh37
NC_000010.9:g.104587001C>G NCBI36
NG_007955.1:g.5280G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.108G>C MANE Select ENSP00000358903.3:p.Leu36=
ENST00000638190.1:c.108G>C ENSP00000492539.1:p.Leu36=
ENST00000638272.1:c.108G>C ENSP00000491508.1:p.Leu36=
ENST00000638971.1:c.108G>C ENSP00000492313.1:p.Leu36=
ENST00000639393.1:c.108G>C ENSP00000492651.1:p.Leu36=
ENST00000369887.3:c.108G>C ENSP00000358903.3:p.Leu36=
ENST00000489268.1:n.161G>C
NM_000102.3:c.108G>C NP_000093.1:p.Leu36=
NM_000102.4:c.108G>C MANE Select NP_000093.1:p.Leu36=
Search 100 bp 5'
Search 100 bp 3'