Canonical Allele Identifier: CA1728472266
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1797450204

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187281A>T , CM000669.2:g.98187281A>T GRCh38
NC_000007.13:g.97816593A>T , CM000669.1:g.97816593A>T GRCh37
NC_000007.12:g.97654529A>T NCBI36
NG_013375.1:g.85397A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+283A>T MANE Select ENSP00000297293.5:n.998+283A>T
ENST00000297293.5:c.998+283A>T ENSP00000297293.5:n.998+283A>T
NM_014916.3:c.998+283A>T NP_055731.2:n.998+283A>T
XM_011515981.1:c.992+283A>T XP_011514283.1:n.992+283A>T
XM_011515981.3:c.992+283A>T XP_011514283.1:n.992+283A>T
NM_014916.4:c.998+283A>T MANE Select NP_055731.2:n.998+283A>T