Canonical Allele Identifier: CA5617004
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs745417361
ExAC: 10:96701771 G / A
gnomAD v2: 10-96701771-G-A
gnomAD v3: 10-94942014-G-A
gnomAD v4: 10-94942014-G-A
COSMIC: COSM3441990
MyVariant Identifiers: chr10:g.96701771G>A (hg19) chr10:g.94942014G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942014G>A , CM000672.2:g.94942014G>A GRCh38
NC_000010.10:g.96701771G>A , CM000672.1:g.96701771G>A GRCh37
NC_000010.9:g.96691761G>A NCBI36
NG_008385.1:g.8357G>A
NG_008385.2:g.8857G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.325G>A MANE Select ENSP00000260682.6:p.Gly109Arg
ENST00000643112.1:c.325G>A ENSP00000496202.1:p.Gly109Arg
ENST00000645207.1:n.478G>A
ENST00000260682.6:c.325G>A ENSP00000260682.6:p.Gly109Arg
ENST00000461906.1:n.350G>A
ENST00000473496.1:n.96G>A
NM_000771.3:c.325G>A NP_000762.2:p.Gly109Arg
NM_000771.4:c.325G>A MANE Select NP_000762.2:p.Gly109Arg
Search 100 bp 5'
Search 100 bp 3'