Canonical Allele Identifier: CA2550128088
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94947514C>G , CM000672.2:g.94947514C>G GRCh38
NC_000010.10:g.96707271C>G , CM000672.1:g.96707271C>G GRCh37
NC_000010.9:g.96697261C>G NCBI36
NG_008385.1:g.13857C>G
NG_008385.2:g.14357C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.482-265C>G MANE Select ENSP00000260682.6:n.482-265C>G
ENST00000643112.1:c.482-265C>G ENSP00000496202.1:n.482-265C>G
ENST00000645207.1:n.635-265C>G
ENST00000260682.6:c.482-265C>G ENSP00000260682.6:n.482-265C>G
ENST00000473496.1:n.253-265C>G
NM_000771.3:c.482-265C>G NP_000762.2:n.482-265C>G
NM_000771.4:c.482-265C>G MANE Select NP_000762.2:n.482-265C>G