Canonical Allele Identifier: CA2683855101
Gene: LMTK2 HGNC NCBI

Linked Data

gnomAD v4: 7-98187050-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187050T>G , CM000669.2:g.98187050T>G GRCh38
NC_000007.13:g.97816362T>G , CM000669.1:g.97816362T>G GRCh37
NC_000007.12:g.97654298T>G NCBI36
NG_013375.1:g.85166T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+52T>G MANE Select ENSP00000297293.5:n.998+52T>G
ENST00000297293.5:c.998+52T>G ENSP00000297293.5:n.998+52T>G
NM_014916.3:c.998+52T>G NP_055731.2:n.998+52T>G
XM_011515981.1:c.992+52T>G XP_011514283.1:n.992+52T>G
XM_011515981.3:c.992+52T>G XP_011514283.1:n.992+52T>G
NM_014916.4:c.998+52T>G MANE Select NP_055731.2:n.998+52T>G
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