Canonical Allele Identifier: CA5617023
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs375198934
ExAC: 10:96701938 C / T
gnomAD v2: 10-96701938-C-T
gnomAD v3: 10-94942181-C-T
gnomAD v4: 10-94942181-C-T
MyVariant Identifiers: chr10:g.96701938C>T (hg19) chr10:g.94942181C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942181C>T , CM000672.2:g.94942181C>T GRCh38
NC_000010.10:g.96701938C>T , CM000672.1:g.96701938C>T GRCh37
NC_000010.9:g.96691928C>T NCBI36
NG_008385.1:g.8524C>T
NG_008385.2:g.9024C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.332-11C>T MANE Select ENSP00000260682.6:n.332-11C>T
ENST00000643112.1:c.332-11C>T ENSP00000496202.1:n.332-11C>T
ENST00000645207.1:n.485-11C>T
ENST00000260682.6:c.332-11C>T ENSP00000260682.6:n.332-11C>T
ENST00000461906.1:n.357-11C>T
ENST00000473496.1:n.103-11C>T
NM_000771.3:c.332-11C>T NP_000762.2:n.332-11C>T
NM_000771.4:c.332-11C>T MANE Select NP_000762.2:n.332-11C>T
Search 100 bp 5'
Search 100 bp 3'