Canonical Allele Identifier: CA377677124
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1302831772
gnomAD v2: 10-96748739-T-G
gnomAD v3: 10-94988982-T-G
gnomAD v4: 10-94988982-T-G
MyVariant Identifiers: chr10:g.96748739T>G (hg19) chr10:g.94988982T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988982T>G , CM000672.2:g.94988982T>G GRCh38
NC_000010.10:g.96748739T>G , CM000672.1:g.96748739T>G GRCh37
NC_000010.9:g.96738729T>G NCBI36
NG_008385.1:g.55325T>G
NG_008385.2:g.55825T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1427T>G MANE Select ENSP00000260682.6:p.Phe476Cys
ENST00000643112.1:c.*436T>G ENSP00000496202.1:n.*436T>G
ENST00000260682.6:c.1427T>G ENSP00000260682.6:p.Phe476Cys
NM_000771.3:c.1427T>G NP_000762.2:p.Phe476Cys
NM_000771.4:c.1427T>G MANE Select NP_000762.2:p.Phe476Cys
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