Canonical Allele Identifier: CA2789072576
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941821T>C , CM000672.2:g.94941821T>C GRCh38
NC_000010.10:g.96701578T>C , CM000672.1:g.96701578T>C GRCh37
NC_000010.9:g.96691568T>C NCBI36
NG_008385.1:g.8164T>C
NG_008385.2:g.8664T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-37T>C MANE Select ENSP00000260682.6:n.169-37T>C
ENST00000643112.1:c.169-37T>C ENSP00000496202.1:n.169-37T>C
ENST00000645207.1:n.285T>C
ENST00000260682.6:c.169-37T>C ENSP00000260682.6:n.169-37T>C
ENST00000461906.1:n.194-37T>C
NM_000771.3:c.169-37T>C NP_000762.2:n.169-37T>C
NM_000771.4:c.169-37T>C MANE Select NP_000762.2:n.169-37T>C
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