Canonical Allele Identifier: CA670187949
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1291777220
gnomAD v3: 10-94989194-C-T
gnomAD v4: 10-94989194-C-T
MyVariant Identifiers: chr10:g.96748951C>T (hg19) chr10:g.94989194C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989194C>T , CM000672.2:g.94989194C>T GRCh38
NC_000010.10:g.96748951C>T , CM000672.1:g.96748951C>T GRCh37
NC_000010.9:g.96738941C>T NCBI36
NG_008385.1:g.55537C>T
NG_008385.2:g.56037C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.*166C>T MANE Select ENSP00000260682.6:n.*166C>T
ENST00000643112.1:c.*648C>T ENSP00000496202.1:n.*648C>T
ENST00000260682.6:c.*166C>T ENSP00000260682.6:n.*166C>T
NM_000771.3:c.*166C>T NP_000762.2:n.*166C>T
NM_000771.4:c.*166C>T MANE Select NP_000762.2:n.*166C>T
Search 100 bp 5'
Search 100 bp 3'