Canonical Allele Identifier: CA1929298181
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1564709858
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949044T>C , CM000672.2:g.94949044T>C GRCh38
NC_000010.10:g.96708801T>C , CM000672.1:g.96708801T>C GRCh37
NC_000010.9:g.96698791T>C NCBI36
NG_008385.1:g.15387T>C
NG_008385.2:g.15887T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-64T>C MANE Select ENSP00000260682.6:n.643-64T>C
ENST00000643112.1:c.643-64T>C ENSP00000496202.1:n.643-64T>C
ENST00000260682.6:c.643-64T>C ENSP00000260682.6:n.643-64T>C
ENST00000473496.1:n.414-64T>C
NM_000771.3:c.643-64T>C NP_000762.2:n.643-64T>C
NM_000771.4:c.643-64T>C MANE Select NP_000762.2:n.643-64T>C
Search 100 bp 5'
Search 100 bp 3'