Canonical Allele Identifier: CA211729481
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs946620122
gnomAD v3: 10-94981097-C-T
gnomAD v4: 10-94981097-C-T
MyVariant Identifiers: chr10:g.96740854C>T (hg19) chr10:g.94981097C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981097C>T , CM000672.2:g.94981097C>T GRCh38
NC_000010.10:g.96740854C>T , CM000672.1:g.96740854C>T GRCh37
NC_000010.9:g.96730844C>T NCBI36
NG_008385.1:g.47440C>T
NG_008385.2:g.47940C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.962-86C>T MANE Select ENSP00000260682.6:n.962-86C>T
ENST00000643112.1:c.820-86C>T ENSP00000496202.1:n.820-86C>T
ENST00000260682.6:c.962-86C>T ENSP00000260682.6:n.962-86C>T
NM_000771.3:c.962-86C>T NP_000762.2:n.962-86C>T
NM_000771.4:c.962-86C>T MANE Select NP_000762.2:n.962-86C>T
Search 100 bp 5'
Search 100 bp 3'