Canonical Allele Identifier: CA2580952638

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981151T>G , CM000672.2:g.94981151T>G	GRCh38
NC_000010.10:g.96740908T>G , CM000672.1:g.96740908T>G	GRCh37
NC_000010.9:g.96730898T>G	NCBI36
NG_008385.1:g.47494T>G
NG_008385.2:g.47994T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.962-32T>G MANE Select	ENSP00000260682.6:n.962-32T>G
ENST00000643112.1:c.820-32T>G	ENSP00000496202.1:n.820-32T>G
ENST00000260682.6:c.962-32T>G	ENSP00000260682.6:n.962-32T>G
NM_000771.3:c.962-32T>G	NP_000762.2:n.962-32T>G
NM_000771.4:c.962-32T>G MANE Select	NP_000762.2:n.962-32T>G