Canonical Allele Identifier: CA931402145
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v3: 10-94974525-G-GTT
gnomAD v4: 10-94974525-G-GTT
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974525_94974526insTT , CM000672.2:g.94974525_94974526insTT GRCh38
NC_000010.10:g.96734282_96734283insTT , CM000672.1:g.96734282_96734283insTT GRCh37
NC_000010.9:g.96724272_96724273insTT NCBI36
NG_008385.1:g.40868_40869insTT
NG_008385.2:g.41368_41369insTT

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.961+2280_961+2281insTT MANE Select ENSP00000260682.6:n.961+2280_961+2281insTT
ENST00000643112.1:c.820-6658_820-6657insTT ENSP00000496202.1:n.820-6658_820-6657insTT
ENST00000260682.6:c.961+2280_961+2281insTT ENSP00000260682.6:n.961+2280_961+2281insTT
NM_000771.3:c.961+2280_961+2281insTT NP_000762.2:n.961+2280_961+2281insTT
NM_000771.4:c.961+2280_961+2281insTT MANE Select NP_000762.2:n.961+2280_961+2281insTT
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