Canonical Allele Identifier: CA377676915
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748640T>A (hg19) chr10:g.94988883T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988883T>A , CM000672.2:g.94988883T>A GRCh38
NC_000010.10:g.96748640T>A , CM000672.1:g.96748640T>A GRCh37
NC_000010.9:g.96738630T>A NCBI36
NG_008385.1:g.55226T>A
NG_008385.2:g.55726T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1328T>A MANE Select ENSP00000260682.6:p.Met443Lys
ENST00000643112.1:c.*337T>A ENSP00000496202.1:n.*337T>A
ENST00000260682.6:c.1328T>A ENSP00000260682.6:p.Met443Lys
NM_000771.3:c.1328T>A NP_000762.2:p.Met443Lys
NM_000771.4:c.1328T>A MANE Select NP_000762.2:p.Met443Lys
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Search 100 bp 3'