Canonical Allele Identifier: CA211735528
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs749767359
gnomAD v2: 10-96748639-A-G
gnomAD v4: 10-94988882-A-G
MyVariant Identifiers: chr10:g.96748639A>G (hg19) chr10:g.94988882A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988882A>G , CM000672.2:g.94988882A>G GRCh38
NC_000010.10:g.96748639A>G , CM000672.1:g.96748639A>G GRCh37
NC_000010.9:g.96738629A>G NCBI36
NG_008385.1:g.55225A>G
NG_008385.2:g.55725A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1327A>G MANE Select ENSP00000260682.6:p.Met443Val
ENST00000643112.1:c.*336A>G ENSP00000496202.1:n.*336A>G
ENST00000260682.6:c.1327A>G ENSP00000260682.6:p.Met443Val
NM_000771.3:c.1327A>G NP_000762.2:p.Met443Val
NM_000771.4:c.1327A>G MANE Select NP_000762.2:p.Met443Val
Search 100 bp 5'
Search 100 bp 3'