Canonical Allele Identifier: CA377672731
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2031392062
MyVariant Identifiers: chr10:g.96701669G>A (hg19) chr10:g.94941912G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941912G>A , CM000672.2:g.94941912G>A GRCh38
NC_000010.10:g.96701669G>A , CM000672.1:g.96701669G>A GRCh37
NC_000010.9:g.96691659G>A NCBI36
NG_008385.1:g.8255G>A
NG_008385.2:g.8755G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.223G>A MANE Select ENSP00000260682.6:p.Val75Met
ENST00000643112.1:c.223G>A ENSP00000496202.1:p.Val75Met
ENST00000645207.1:n.376G>A
ENST00000260682.6:c.223G>A ENSP00000260682.6:p.Val75Met
ENST00000461906.1:n.248G>A
NM_000771.3:c.223G>A NP_000762.2:p.Val75Met
NM_000771.4:c.223G>A MANE Select NP_000762.2:p.Val75Met
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