Canonical Allele Identifier: CA1104852687
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1797450044
gnomAD v3: 7-98187272-A-C
gnomAD v4: 7-98187272-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187272A>C , CM000669.2:g.98187272A>C GRCh38
NC_000007.13:g.97816584A>C , CM000669.1:g.97816584A>C GRCh37
NC_000007.12:g.97654520A>C NCBI36
NG_013375.1:g.85388A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+274A>C MANE Select ENSP00000297293.5:n.998+274A>C
ENST00000297293.5:c.998+274A>C ENSP00000297293.5:n.998+274A>C
NM_014916.3:c.998+274A>C NP_055731.2:n.998+274A>C
XM_011515981.1:c.992+274A>C XP_011514283.1:n.992+274A>C
XM_011515981.3:c.992+274A>C XP_011514283.1:n.992+274A>C
NM_014916.4:c.998+274A>C MANE Select NP_055731.2:n.998+274A>C
Search 100 bp 5'
Search 100 bp 3'