Canonical Allele Identifier: CA377676984

Gene: CYP2C9

Linked Data

• dbSNP Id: rs748356078
• MyVariant Identifiers: chr10:g.96748673A>T (hg19) ; chr10:g.94988916A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94988916A>T , CM000672.2:g.94988916A>T	GRCh38
NC_000010.10:g.96748673A>T , CM000672.1:g.96748673A>T	GRCh37
NC_000010.9:g.96738663A>T	NCBI36
NG_008385.1:g.55259A>T
NG_008385.2:g.55759A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1361A>T MANE Select	ENSP00000260682.6:p.Gln454Leu
ENST00000643112.1:c.*370A>T	ENSP00000496202.1:n.*370A>T
ENST00000260682.6:c.1361A>T	ENSP00000260682.6:p.Gln454Leu
NM_000771.3:c.1361A>T	NP_000762.2:p.Gln454Leu
NM_000771.4:c.1361A>T MANE Select	NP_000762.2:p.Gln454Leu