Canonical Allele Identifier: CA1929292658
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1564707781
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942712G>C , CM000672.2:g.94942712G>C GRCh38
NC_000010.10:g.96702469G>C , CM000672.1:g.96702469G>C GRCh37
NC_000010.9:g.96692459G>C NCBI36
NG_008385.1:g.9055G>C
NG_008385.2:g.9555G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+371G>C MANE Select ENSP00000260682.6:n.481+371G>C
ENST00000643112.1:c.481+371G>C ENSP00000496202.1:n.481+371G>C
ENST00000645207.1:n.634+371G>C
ENST00000260682.6:c.481+371G>C ENSP00000260682.6:n.481+371G>C
ENST00000461906.1:n.877G>C
ENST00000473496.1:n.252+371G>C
NM_000771.3:c.481+371G>C NP_000762.2:n.481+371G>C
NM_000771.4:c.481+371G>C MANE Select NP_000762.2:n.481+371G>C
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