Canonical Allele Identifier: CA377673449

Gene: CYP2C9

Linked Data

• MyVariant Identifiers: chr10:g.96702100T>A (hg19) ; chr10:g.94942343T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942343T>A , CM000672.2:g.94942343T>A	GRCh38
NC_000010.10:g.96702100T>A , CM000672.1:g.96702100T>A	GRCh37
NC_000010.9:g.96692090T>A	NCBI36
NG_008385.1:g.8686T>A
NG_008385.2:g.9186T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.481+2T>A MANE Select	ENSP00000260682.6:n.481+2T>A
ENST00000643112.1:c.481+2T>A	ENSP00000496202.1:n.481+2T>A
ENST00000645207.1:n.634+2T>A
ENST00000260682.6:c.481+2T>A	ENSP00000260682.6:n.481+2T>A
ENST00000461906.1:n.508T>A
ENST00000473496.1:n.252+2T>A
NM_000771.3:c.481+2T>A	NP_000762.2:n.481+2T>A
NM_000771.4:c.481+2T>A MANE Select	NP_000762.2:n.481+2T>A