Canonical Allele Identifier: CA1728472246
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1797449433

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187228A>G , CM000669.2:g.98187228A>G GRCh38
NC_000007.13:g.97816540A>G , CM000669.1:g.97816540A>G GRCh37
NC_000007.12:g.97654476A>G NCBI36
NG_013375.1:g.85344A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+230A>G MANE Select ENSP00000297293.5:n.998+230A>G
ENST00000297293.5:c.998+230A>G ENSP00000297293.5:n.998+230A>G
NM_014916.3:c.998+230A>G NP_055731.2:n.998+230A>G
XM_011515981.1:c.992+230A>G XP_011514283.1:n.992+230A>G
XM_011515981.3:c.992+230A>G XP_011514283.1:n.992+230A>G
NM_014916.4:c.998+230A>G MANE Select NP_055731.2:n.998+230A>G