Canonical Allele Identifier: CA1929341815
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2032225150
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981148T>C , CM000672.2:g.94981148T>C GRCh38
NC_000010.10:g.96740905T>C , CM000672.1:g.96740905T>C GRCh37
NC_000010.9:g.96730895T>C NCBI36
NG_008385.1:g.47491T>C
NG_008385.2:g.47991T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.962-35T>C MANE Select ENSP00000260682.6:n.962-35T>C
ENST00000643112.1:c.820-35T>C ENSP00000496202.1:n.820-35T>C
ENST00000260682.6:c.962-35T>C ENSP00000260682.6:n.962-35T>C
NM_000771.3:c.962-35T>C NP_000762.2:n.962-35T>C
NM_000771.4:c.962-35T>C MANE Select NP_000762.2:n.962-35T>C
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