Canonical Allele Identifier: CA5617063
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs7900194

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942309G>T , CM000672.2:g.94942309G>T GRCh38
NC_000010.10:g.96702066G>T , CM000672.1:g.96702066G>T GRCh37
NC_000010.9:g.96692056G>T NCBI36
NG_008385.1:g.8652G>T
NG_008385.2:g.9152G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.449G>T MANE Select ENSP00000260682.6:p.Arg150Leu
ENST00000643112.1:c.449G>T ENSP00000496202.1:p.Arg150Leu
ENST00000645207.1:n.602G>T
ENST00000260682.6:c.449G>T ENSP00000260682.6:p.Arg150Leu
ENST00000461906.1:n.474G>T
ENST00000473496.1:n.220G>T
NM_000771.3:c.449G>T NP_000762.2:p.Arg150Leu
NM_000771.4:c.449G>T MANE Select NP_000762.2:p.Arg150Leu