Canonical Allele Identifier: CA1929342530

Gene: CYP2C9

Linked Data

• dbSNP Id: rs2032235464

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981631T>G , CM000672.2:g.94981631T>G	GRCh38
NC_000010.10:g.96741388T>G , CM000672.1:g.96741388T>G	GRCh37
NC_000010.9:g.96731378T>G	NCBI36
NG_008385.1:g.47974T>G
NG_008385.2:g.48474T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1149+261T>G MANE Select	ENSP00000260682.6:n.1149+261T>G
ENST00000643112.1:c.*158+261T>G	ENSP00000496202.1:n.*158+261T>G
ENST00000260682.6:c.1149+261T>G	ENSP00000260682.6:n.1149+261T>G
NM_000771.3:c.1149+261T>G	NP_000762.2:n.1149+261T>G
NM_000771.4:c.1149+261T>G MANE Select	NP_000762.2:n.1149+261T>G