Canonical Allele Identifier: CA2683855173
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs2116452370
gnomAD v4: 7-98187147-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187147C>T , CM000669.2:g.98187147C>T GRCh38
NC_000007.13:g.97816459C>T , CM000669.1:g.97816459C>T GRCh37
NC_000007.12:g.97654395C>T NCBI36
NG_013375.1:g.85263C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+149C>T MANE Select ENSP00000297293.5:n.998+149C>T
ENST00000297293.5:c.998+149C>T ENSP00000297293.5:n.998+149C>T
NM_014916.3:c.998+149C>T NP_055731.2:n.998+149C>T
XM_011515981.1:c.992+149C>T XP_011514283.1:n.992+149C>T
XM_011515981.3:c.992+149C>T XP_011514283.1:n.992+149C>T
NM_014916.4:c.998+149C>T MANE Select NP_055731.2:n.998+149C>T