Canonical Allele Identifier: CA1929296064
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2031514304
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94947319T>C , CM000672.2:g.94947319T>C GRCh38
NC_000010.10:g.96707076T>C , CM000672.1:g.96707076T>C GRCh37
NC_000010.9:g.96697066T>C NCBI36
NG_008385.1:g.13662T>C
NG_008385.2:g.14162T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.482-460T>C MANE Select ENSP00000260682.6:n.482-460T>C
ENST00000643112.1:c.482-460T>C ENSP00000496202.1:n.482-460T>C
ENST00000645207.1:n.635-460T>C
ENST00000260682.6:c.482-460T>C ENSP00000260682.6:n.482-460T>C
ENST00000473496.1:n.253-460T>C
NM_000771.3:c.482-460T>C NP_000762.2:n.482-460T>C
NM_000771.4:c.482-460T>C MANE Select NP_000762.2:n.482-460T>C
Search 100 bp 5'
Search 100 bp 3'