Canonical Allele Identifier: CA247515484
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1043987934
MyVariant Identifiers: chr13:g.33610387C>A (hg19) chr13:g.33036250C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036250C>A , CM000675.2:g.33036250C>A GRCh38
NC_000013.10:g.33610387C>A , CM000675.1:g.33610387C>A GRCh37
NC_000013.9:g.32508387C>A NCBI36
NG_011485.1:g.24817C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17517C>A MANE Select ENSP00000369442.3:n.820-17517C>A
ENST00000380099.3:c.820-17517C>A ENSP00000369442.3:n.820-17517C>A
ENST00000487852.1:n.828-17517C>A
NM_004795.3:c.820-17517C>A NP_004786.2:n.820-17517C>A
XM_006719895.1:c.-102-17517C>A XP_006719958.1:n.-102-17517C>A
XM_006719895.2:c.-102-17517C>A XP_006719958.1:n.-102-17517C>A
NM_004795.4:c.820-17517C>A MANE Select NP_004786.2:n.820-17517C>A
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