Canonical Allele Identifier: CA377672974
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942196T>G , CM000672.2:g.94942196T>G GRCh38
NC_000010.10:g.96701953T>G , CM000672.1:g.96701953T>G GRCh37
NC_000010.9:g.96691943T>G NCBI36
NG_008385.1:g.8539T>G
NG_008385.2:g.9039T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.336T>G MANE Select ENSP00000260682.6:p.Ile112Met
ENST00000643112.1:c.336T>G ENSP00000496202.1:p.Ile112Met
ENST00000645207.1:n.489T>G
ENST00000260682.6:c.336T>G ENSP00000260682.6:p.Ile112Met
ENST00000461906.1:n.361T>G
ENST00000473496.1:n.107T>G
NM_000771.3:c.336T>G NP_000762.2:p.Ile112Met
NM_000771.4:c.336T>G MANE Select NP_000762.2:p.Ile112Met