Canonical Allele Identifier: CA1929341885
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981191_94981192delinsCA , CM000672.2:g.94981191_94981192delinsCA GRCh38
NC_000010.10:g.96740948_96740949delinsCA , CM000672.1:g.96740948_96740949delinsCA GRCh37
NC_000010.9:g.96730938_96730939delinsCA NCBI36
NG_008385.1:g.47534_47535delinsCA
NG_008385.2:g.48034_48035delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.970_971delinsCA MANE Select ENSP00000260682.6:p.Gln324=
ENST00000643112.1:c.828_829delinsCA ENSP00000496202.1:p.Ser276=
ENST00000260682.6:c.970_971delinsCA ENSP00000260682.6:p.Gln324=
NM_000771.3:c.970_971delinsCA NP_000762.2:p.Gln324=
NM_000771.4:c.970_971delinsCA MANE Select NP_000762.2:p.Gln324=
Search 100 bp 5'
Search 100 bp 3'