Canonical Allele Identifier: CA309911210
Gene: KIR2DL4 HGNC NCBI

Linked Data

dbSNP Id: rs631717
gnomAD v3: 19-54811520-G-A
gnomAD v4: 19-54811520-G-A
MyVariant Identifiers: chr19:g.54811520G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54811520G>A , CM000681.2:g.54811520G>A GRCh38
NC_000019.8:g.60014787G>A NCBI36
NG_021414.1:g.83G>A
NG_021414.2:g.83G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000345540.10:c.707-2170G>A MANE Select ENSP00000339634.5:n.707-2170G>A
ENST00000345540.9:c.707-2170G>A ENSP00000339634.5:n.707-2170G>A
ENST00000346587.8:c.422-2170G>A ENSP00000345331.4:n.422-2170G>A
ENST00000357494.8:c.656-2170G>A ENSP00000350088.4:n.656-2170G>A
ENST00000359085.8:c.707-1605G>A ENSP00000351988.4:n.707-1605G>A
ENST00000396284.6:c.824-1605G>A ENSP00000379580.3:n.824-1605G>A
ENST00000396289.5:c.702-1605G>A
ENST00000396293.5:c.371-2170G>A ENSP00000379588.1:n.371-2170G>A
ENST00000463062.1:n.668-1605G>A
ENST00000486965.6:n.667-2322G>A
NM_001080770.1:c.707-2170G>A NP_001074239.1:n.707-2170G>A
NM_001080772.1:c.707-1605G>A NP_001074241.1:n.707-1605G>A
XR_430260.1:n.690+4688C>T
NM_001080770.2:c.707-2170G>A MANE Select NP_001074239.1:n.707-2170G>A
NM_001080772.2:c.707-1605G>A NP_001074241.1:n.707-1605G>A
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