Canonical Allele Identifier: CA2683855110
Gene: LMTK2 HGNC NCBI

Linked Data

gnomAD v4: 7-98187059-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187059T>C , CM000669.2:g.98187059T>C GRCh38
NC_000007.13:g.97816371T>C , CM000669.1:g.97816371T>C GRCh37
NC_000007.12:g.97654307T>C NCBI36
NG_013375.1:g.85175T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+61T>C MANE Select ENSP00000297293.5:n.998+61T>C
ENST00000297293.5:c.998+61T>C ENSP00000297293.5:n.998+61T>C
NM_014916.3:c.998+61T>C NP_055731.2:n.998+61T>C
XM_011515981.1:c.992+61T>C XP_011514283.1:n.992+61T>C
XM_011515981.3:c.992+61T>C XP_011514283.1:n.992+61T>C
NM_014916.4:c.998+61T>C MANE Select NP_055731.2:n.998+61T>C
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