Canonical Allele Identifier: CA377672976
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942197G>C , CM000672.2:g.94942197G>C GRCh38
NC_000010.10:g.96701954G>C , CM000672.1:g.96701954G>C GRCh37
NC_000010.9:g.96691944G>C NCBI36
NG_008385.1:g.8540G>C
NG_008385.2:g.9040G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.337G>C MANE Select ENSP00000260682.6:p.Val113Leu
ENST00000643112.1:c.337G>C ENSP00000496202.1:p.Val113Leu
ENST00000645207.1:n.490G>C
ENST00000260682.6:c.337G>C ENSP00000260682.6:p.Val113Leu
ENST00000461906.1:n.362G>C
ENST00000473496.1:n.108G>C
NM_000771.3:c.337G>C NP_000762.2:p.Val113Leu
NM_000771.4:c.337G>C MANE Select NP_000762.2:p.Val113Leu