Canonical Allele Identifier: CA2610266396
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94981039-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981042del , CM000672.2:g.94981042del GRCh38
NC_000010.10:g.96740799del , CM000672.1:g.96740799del GRCh37
NC_000010.9:g.96730789del NCBI36
NG_008385.1:g.47385del
NG_008385.2:g.47885del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.962-141del MANE Select ENSP00000260682.6:n.962-141del
ENST00000643112.1:c.820-141del ENSP00000496202.1:n.820-141del
ENST00000260682.6:c.962-141del ENSP00000260682.6:n.962-141del
NM_000771.3:c.962-141del NP_000762.2:n.962-141del
NM_000771.4:c.962-141del MANE Select NP_000762.2:n.962-141del
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