Canonical Allele Identifier: CA377676392
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1371272359
gnomAD v3: 10-94981315-G-T
gnomAD v4: 10-94981315-G-T
MyVariant Identifiers: chr10:g.96741072G>T (hg19) chr10:g.94981315G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981315G>T , CM000672.2:g.94981315G>T GRCh38
NC_000010.10:g.96741072G>T , CM000672.1:g.96741072G>T GRCh37
NC_000010.9:g.96731062G>T NCBI36
NG_008385.1:g.47658G>T
NG_008385.2:g.48158G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1094G>T MANE Select ENSP00000260682.6:p.Ser365Ile
ENST00000643112.1:c.*103G>T ENSP00000496202.1:n.*103G>T
ENST00000260682.6:c.1094G>T ENSP00000260682.6:p.Ser365Ile
NM_000771.3:c.1094G>T NP_000762.2:p.Ser365Ile
NM_000771.4:c.1094G>T MANE Select NP_000762.2:p.Ser365Ile
Search 100 bp 5'
Search 100 bp 3'