Canonical Allele Identifier: CA1104852643
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1797447868
gnomAD v3: 7-98187135-G-C
gnomAD v4: 7-98187135-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187135G>C , CM000669.2:g.98187135G>C GRCh38
NC_000007.13:g.97816447G>C , CM000669.1:g.97816447G>C GRCh37
NC_000007.12:g.97654383G>C NCBI36
NG_013375.1:g.85251G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+137G>C MANE Select ENSP00000297293.5:n.998+137G>C
ENST00000297293.5:c.998+137G>C ENSP00000297293.5:n.998+137G>C
NM_014916.3:c.998+137G>C NP_055731.2:n.998+137G>C
XM_011515981.1:c.992+137G>C XP_011514283.1:n.992+137G>C
XM_011515981.3:c.992+137G>C XP_011514283.1:n.992+137G>C
NM_014916.4:c.998+137G>C MANE Select NP_055731.2:n.998+137G>C
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