Canonical Allele Identifier: CA670182669

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1246136851
• MyVariant Identifiers: chr10:g.96740904C>T (hg19) ; chr10:g.94981147C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981147C>T , CM000672.2:g.94981147C>T	GRCh38
NC_000010.10:g.96740904C>T , CM000672.1:g.96740904C>T	GRCh37
NC_000010.9:g.96730894C>T	NCBI36
NG_008385.1:g.47490C>T
NG_008385.2:g.47990C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.962-36C>T MANE Select	ENSP00000260682.6:n.962-36C>T
ENST00000643112.1:c.820-36C>T	ENSP00000496202.1:n.820-36C>T
ENST00000260682.6:c.962-36C>T	ENSP00000260682.6:n.962-36C>T
NM_000771.3:c.962-36C>T	NP_000762.2:n.962-36C>T
NM_000771.4:c.962-36C>T MANE Select	NP_000762.2:n.962-36C>T