Canonical Allele Identifier: CA211735620
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1003261227
gnomAD v2: 10-96748742-C-T
gnomAD v4: 10-94988985-C-T
MyVariant Identifiers: chr10:g.96748742C>T (hg19) chr10:g.94988985C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988985C>T , CM000672.2:g.94988985C>T GRCh38
NC_000010.10:g.96748742C>T , CM000672.1:g.96748742C>T GRCh37
NC_000010.9:g.96738732C>T NCBI36
NG_008385.1:g.55328C>T
NG_008385.2:g.55828C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1430C>T MANE Select ENSP00000260682.6:p.Ala477Val
ENST00000643112.1:c.*439C>T ENSP00000496202.1:n.*439C>T
ENST00000260682.6:c.1430C>T ENSP00000260682.6:p.Ala477Val
NM_000771.3:c.1430C>T NP_000762.2:p.Ala477Val
NM_000771.4:c.1430C>T MANE Select NP_000762.2:p.Ala477Val
Search 100 bp 5'
Search 100 bp 3'