Canonical Allele Identifier: CA377673037
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94942222-A-G
MyVariant Identifiers: chr10:g.96701979A>G (hg19) chr10:g.94942222A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942222A>G , CM000672.2:g.94942222A>G GRCh38
NC_000010.10:g.96701979A>G , CM000672.1:g.96701979A>G GRCh37
NC_000010.9:g.96691969A>G NCBI36
NG_008385.1:g.8565A>G
NG_008385.2:g.9065A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.362A>G MANE Select ENSP00000260682.6:p.Lys121Arg
ENST00000643112.1:c.362A>G ENSP00000496202.1:p.Lys121Arg
ENST00000645207.1:n.515A>G
ENST00000260682.6:c.362A>G ENSP00000260682.6:p.Lys121Arg
ENST00000461906.1:n.387A>G
ENST00000473496.1:n.133A>G
NM_000771.3:c.362A>G NP_000762.2:p.Lys121Arg
NM_000771.4:c.362A>G MANE Select NP_000762.2:p.Lys121Arg
Search 100 bp 5'
Search 100 bp 3'