Canonical Allele Identifier: CA670159104
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1319480232

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942347T>G , CM000672.2:g.94942347T>G GRCh38
NC_000010.10:g.96702104T>G , CM000672.1:g.96702104T>G GRCh37
NC_000010.9:g.96692094T>G NCBI36
NG_008385.1:g.8690T>G
NG_008385.2:g.9190T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+6T>G MANE Select ENSP00000260682.6:n.481+6T>G
ENST00000643112.1:c.481+6T>G ENSP00000496202.1:n.481+6T>G
ENST00000645207.1:n.634+6T>G
ENST00000260682.6:c.481+6T>G ENSP00000260682.6:n.481+6T>G
ENST00000461906.1:n.512T>G
ENST00000473496.1:n.252+6T>G
NM_000771.3:c.481+6T>G NP_000762.2:n.481+6T>G
NM_000771.4:c.481+6T>G MANE Select NP_000762.2:n.481+6T>G