Canonical Allele Identifier: CA5617271
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs780145404
ExAC: 10:96740951 G / A
gnomAD v2: 10-96740951-G-A
gnomAD v4: 10-94981194-G-A
MyVariant Identifiers: chr10:g.96740951G>A (hg19) chr10:g.94981194G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981194G>A , CM000672.2:g.94981194G>A GRCh38
NC_000010.10:g.96740951G>A , CM000672.1:g.96740951G>A GRCh37
NC_000010.9:g.96730941G>A NCBI36
NG_008385.1:g.47537G>A
NG_008385.2:g.48037G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.973G>A MANE Select ENSP00000260682.6:p.Glu325Lys
ENST00000643112.1:c.831G>A ENSP00000496202.1:p.Arg277=
ENST00000260682.6:c.973G>A ENSP00000260682.6:p.Glu325Lys
NM_000771.3:c.973G>A NP_000762.2:p.Glu325Lys
NM_000771.4:c.973G>A MANE Select NP_000762.2:p.Glu325Lys
Search 100 bp 5'
Search 100 bp 3'