Canonical Allele Identifier: CA609105144
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1404833965
gnomAD v2: 13-33598790-C-A
gnomAD v3: 13-33024652-C-A
gnomAD v4: 13-33024652-C-A
MyVariant Identifiers: chr13:g.33598790C>A (hg19) chr13:g.33024652C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33024652C>A , CM000675.2:g.33024652C>A GRCh38
NC_000013.10:g.33598790C>A , CM000675.1:g.33598790C>A GRCh37
NC_000013.9:g.32496790C>A NCBI36
NG_011485.1:g.13220C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.819+7393C>A MANE Select ENSP00000369442.3:n.819+7393C>A
ENST00000380099.3:c.819+7393C>A ENSP00000369442.3:n.819+7393C>A
ENST00000487852.1:n.827+7393C>A
NM_004795.3:c.819+7393C>A NP_004786.2:n.819+7393C>A
XM_006719895.1:c.-103+8339C>A XP_006719958.1:n.-103+8339C>A
XM_006719895.2:c.-103+8339C>A XP_006719958.1:n.-103+8339C>A
NM_004795.4:c.819+7393C>A MANE Select NP_004786.2:n.819+7393C>A
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