Canonical Allele Identifier: CA595316237
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1446803116
gnomAD v2: 10-96708850-ATTG-A
gnomAD v3: 10-94949093-ATTG-A
gnomAD v4: 10-94949093-ATTG-A
MyVariant Identifiers: chr10:g.96708851_96708853del (hg19) chr10:g.94949094_94949096del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949096_94949098del , CM000672.2:g.94949096_94949098del GRCh38
NC_000010.10:g.96708853_96708855del , CM000672.1:g.96708853_96708855del GRCh37
NC_000010.9:g.96698843_96698845del NCBI36
NG_008385.1:g.15439_15441del
NG_008385.2:g.15939_15941del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-12_643-10del MANE Select ENSP00000260682.6:n.643-12_643-10del
ENST00000643112.1:c.643-12_643-10del ENSP00000496202.1:n.643-12_643-10del
ENST00000260682.6:c.643-12_643-10del ENSP00000260682.6:n.643-12_643-10del
ENST00000473496.1:n.414-12_414-10del
NM_000771.3:c.643-12_643-10del NP_000762.2:n.643-12_643-10del
NM_000771.4:c.643-12_643-10del MANE Select NP_000762.2:n.643-12_643-10del
Search 100 bp 5'
Search 100 bp 3'