Canonical Allele Identifier: CA2610266445
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94981112-TAC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981113_94981114del , CM000672.2:g.94981113_94981114del GRCh38
NC_000010.10:g.96740870_96740871del , CM000672.1:g.96740870_96740871del GRCh37
NC_000010.9:g.96730860_96730861del NCBI36
NG_008385.1:g.47456_47457del
NG_008385.2:g.47956_47957del

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.962-70_962-69del MANE Select ENSP00000260682.6:n.962-70_962-69del
ENST00000643112.1:c.820-70_820-69del ENSP00000496202.1:n.820-70_820-69del
ENST00000260682.6:c.962-70_962-69del ENSP00000260682.6:n.962-70_962-69del
NM_000771.3:c.962-70_962-69del NP_000762.2:n.962-70_962-69del
NM_000771.4:c.962-70_962-69del MANE Select NP_000762.2:n.962-70_962-69del
Search 100 bp 5'
Search 100 bp 3'