Canonical Allele Identifier: CA2610266451

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94981128-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981128C>T , CM000672.2:g.94981128C>T	GRCh38
NC_000010.10:g.96740885C>T , CM000672.1:g.96740885C>T	GRCh37
NC_000010.9:g.96730875C>T	NCBI36
NG_008385.1:g.47471C>T
NG_008385.2:g.47971C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.962-55C>T MANE Select	ENSP00000260682.6:n.962-55C>T
ENST00000643112.1:c.820-55C>T	ENSP00000496202.1:n.820-55C>T
ENST00000260682.6:c.962-55C>T	ENSP00000260682.6:n.962-55C>T
NM_000771.3:c.962-55C>T	NP_000762.2:n.962-55C>T
NM_000771.4:c.962-55C>T MANE Select	NP_000762.2:n.962-55C>T