Canonical Allele Identifier: CA697439979
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1230935844

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33035954T>G , CM000675.2:g.33035954T>G GRCh38
NC_000013.10:g.33610091T>G , CM000675.1:g.33610091T>G GRCh37
NC_000013.9:g.32508091T>G NCBI36
NG_011485.1:g.24521T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17813T>G MANE Select ENSP00000369442.3:n.820-17813T>G
ENST00000380099.3:c.820-17813T>G ENSP00000369442.3:n.820-17813T>G
ENST00000487852.1:n.828-17813T>G
NM_004795.3:c.820-17813T>G NP_004786.2:n.820-17813T>G
XM_006719895.1:c.-102-17813T>G XP_006719958.1:n.-102-17813T>G
XM_006719895.2:c.-102-17813T>G XP_006719958.1:n.-102-17813T>G
NM_004795.4:c.820-17813T>G MANE Select NP_004786.2:n.820-17813T>G