Canonical Allele Identifier: CA670162502
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1340610336
gnomAD v4: 10-94949101-C-T
MyVariant Identifiers: chr10:g.96708858C>T (hg19) chr10:g.94949101C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949101C>T , CM000672.2:g.94949101C>T GRCh38
NC_000010.10:g.96708858C>T , CM000672.1:g.96708858C>T GRCh37
NC_000010.9:g.96698848C>T NCBI36
NG_008385.1:g.15444C>T
NG_008385.2:g.15944C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-7C>T MANE Select ENSP00000260682.6:n.643-7C>T
ENST00000643112.1:c.643-7C>T ENSP00000496202.1:n.643-7C>T
ENST00000260682.6:c.643-7C>T ENSP00000260682.6:n.643-7C>T
ENST00000473496.1:n.414-7C>T
NM_000771.3:c.643-7C>T NP_000762.2:n.643-7C>T
NM_000771.4:c.643-7C>T MANE Select NP_000762.2:n.643-7C>T
Search 100 bp 5'
Search 100 bp 3'