Canonical Allele Identifier: CA1427079361
Gene: KNG1 HGNC NCBI

Linked Data

dbSNP Id: rs1720097843
gnomAD v4: 3-186718613-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186718613G>A , CM000665.2:g.186718613G>A GRCh38
NC_000003.11:g.186436402G>A , CM000665.1:g.186436402G>A GRCh37
NC_000003.10:g.187919096G>A NCBI36
NG_016009.1:g.6305G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287611.8:c.195+876G>A ENSP00000287611.2:n.195+876G>A
ENST00000644859.2:c.195+876G>A MANE Select ENSP00000493985.1:n.195+876G>A
ENST00000645544.1:n.338+876G>A
ENST00000265023.8:c.195+876G>A ENSP00000265023.4:n.195+876G>A
ENST00000287611.6:c.195+876G>A ENSP00000287611.2:n.195+876G>A
ENST00000447445.1:c.195+876G>A ENSP00000396025.1:n.195+876G>A
NM_000893.3:c.195+876G>A NP_000884.1:n.195+876G>A
NM_001102416.2:c.195+876G>A NP_001095886.1:n.195+876G>A
NM_001166451.1:c.195+876G>A NP_001159923.1:n.195+876G>A
NM_000893.4:c.195+876G>A NP_000884.1:n.195+876G>A
NM_001102416.3:c.195+876G>A MANE Select NP_001095886.1:n.195+876G>A
NM_001166451.2:c.195+876G>A NP_001159923.1:n.195+876G>A
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