Canonical Allele Identifier: CA6944007
Gene: KL HGNC NCBI

Linked Data

ClinVar Variation Id: 311689
ClinVar RCV Id: RCV000261457 RCV001850646
dbSNP Id: rs143344388
ExAC: 13:33628051 G / A
gnomAD v2: 13-33628051-G-A
gnomAD v3: 13-33053914-G-A
gnomAD v4: 13-33053914-G-A
MyVariant Identifiers: chr13:g.33628051G>A (hg19) chr13:g.33053914G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33053914G>A , CM000675.2:g.33053914G>A GRCh38
NC_000013.10:g.33628051G>A , CM000675.1:g.33628051G>A GRCh37
NC_000013.9:g.32526051G>A NCBI36
NG_011485.1:g.42481G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.967G>A MANE Select ENSP00000369442.3:p.Val323Ile
ENST00000380099.3:c.967G>A ENSP00000369442.3:p.Val323Ile
ENST00000487852.1:n.975G>A
NM_004795.3:c.967G>A NP_004786.2:p.Val323Ile
XM_006719895.1:c.46G>A XP_006719958.1:p.Val16Ile
XM_006719895.2:c.46G>A XP_006719958.1:p.Val16Ile
NM_004795.4:c.967G>A MANE Select NP_004786.2:p.Val323Ile
Search 100 bp 5'
Search 100 bp 3'