Canonical Allele Identifier: CA211698493
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs528664778
gnomAD v2: 10-96707197-C-T
gnomAD v3: 10-94947440-C-T
gnomAD v4: 10-94947440-C-T
MyVariant Identifiers: chr10:g.96707197C>T (hg19) chr10:g.94947440C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94947440C>T , CM000672.2:g.94947440C>T GRCh38
NC_000010.10:g.96707197C>T , CM000672.1:g.96707197C>T GRCh37
NC_000010.9:g.96697187C>T NCBI36
NG_008385.1:g.13783C>T
NG_008385.2:g.14283C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.482-339C>T MANE Select ENSP00000260682.6:n.482-339C>T
ENST00000643112.1:c.482-339C>T ENSP00000496202.1:n.482-339C>T
ENST00000645207.1:n.635-339C>T
ENST00000260682.6:c.482-339C>T ENSP00000260682.6:n.482-339C>T
ENST00000473496.1:n.253-339C>T
NM_000771.3:c.482-339C>T NP_000762.2:n.482-339C>T
NM_000771.4:c.482-339C>T MANE Select NP_000762.2:n.482-339C>T
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Search 100 bp 3'