Canonical Allele Identifier: CA377676189
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94981216-G-T
MyVariant Identifiers: chr10:g.96740973G>T (hg19) chr10:g.94981216G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981216G>T , CM000672.2:g.94981216G>T GRCh38
NC_000010.10:g.96740973G>T , CM000672.1:g.96740973G>T GRCh37
NC_000010.9:g.96730963G>T NCBI36
NG_008385.1:g.47559G>T
NG_008385.2:g.48059G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.995G>T MANE Select ENSP00000260682.6:p.Gly332Val
ENST00000643112.1:c.*4G>T ENSP00000496202.1:n.*4G>T
ENST00000260682.6:c.995G>T ENSP00000260682.6:p.Gly332Val
NM_000771.3:c.995G>T NP_000762.2:p.Gly332Val
NM_000771.4:c.995G>T MANE Select NP_000762.2:p.Gly332Val
Search 100 bp 5'
Search 100 bp 3'