Canonical Allele Identifier: CA211724794

Gene: CYP2C9

Linked Data

• dbSNP Id: rs553150888
• MyVariant Identifiers: chr10:g.96734381G>T (hg19) ; chr10:g.94974624G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94974624G>T , CM000672.2:g.94974624G>T	GRCh38
NC_000010.10:g.96734381G>T , CM000672.1:g.96734381G>T	GRCh37
NC_000010.9:g.96724371G>T	NCBI36
NG_008385.1:g.40967G>T
NG_008385.2:g.41467G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.961+2379G>T MANE Select	ENSP00000260682.6:n.961+2379G>T
ENST00000643112.1:c.820-6559G>T	ENSP00000496202.1:n.820-6559G>T
ENST00000260682.6:c.961+2379G>T	ENSP00000260682.6:n.961+2379G>T
NM_000771.3:c.961+2379G>T	NP_000762.2:n.961+2379G>T
NM_000771.4:c.961+2379G>T MANE Select	NP_000762.2:n.961+2379G>T