Canonical Allele Identifier: CA5617398
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs780696025
ExAC: 10:96748661 C / T
gnomAD v2: 10-96748661-C-T
gnomAD v4: 10-94988904-C-T
MyVariant Identifiers: chr10:g.96748661C>T (hg19) chr10:g.94988904C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988904C>T , CM000672.2:g.94988904C>T GRCh38
NC_000010.10:g.96748661C>T , CM000672.1:g.96748661C>T GRCh37
NC_000010.9:g.96738651C>T NCBI36
NG_008385.1:g.55247C>T
NG_008385.2:g.55747C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1349C>T MANE Select ENSP00000260682.6:p.Thr450Ile
ENST00000643112.1:c.*358C>T ENSP00000496202.1:n.*358C>T
ENST00000260682.6:c.1349C>T ENSP00000260682.6:p.Thr450Ile
NM_000771.3:c.1349C>T NP_000762.2:p.Thr450Ile
NM_000771.4:c.1349C>T MANE Select NP_000762.2:p.Thr450Ile
Search 100 bp 5'
Search 100 bp 3'