Canonical Allele Identifier: CA931385252
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2031549298
gnomAD v3: 10-94948861-TA-T
gnomAD v4: 10-94948861-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94948866del , CM000672.2:g.94948866del GRCh38
NC_000010.10:g.96708623del , CM000672.1:g.96708623del GRCh37
NC_000010.9:g.96698613del NCBI36
NG_008385.1:g.15209del
NG_008385.2:g.15709del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-242del MANE Select ENSP00000260682.6:n.643-242del
ENST00000643112.1:c.643-242del ENSP00000496202.1:n.643-242del
ENST00000260682.6:c.643-242del ENSP00000260682.6:n.643-242del
ENST00000473496.1:n.414-242del
NM_000771.3:c.643-242del NP_000762.2:n.643-242del
NM_000771.4:c.643-242del MANE Select NP_000762.2:n.643-242del
Search 100 bp 5'
Search 100 bp 3'