Canonical Allele Identifier: CA163034614
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1001812622
gnomAD v3: 7-98187174-A-G
gnomAD v4: 7-98187174-A-G
MyVariant Identifiers: chr7:g.97816486A>G (hg19) chr7:g.98187174A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187174A>G , CM000669.2:g.98187174A>G GRCh38
NC_000007.13:g.97816486A>G , CM000669.1:g.97816486A>G GRCh37
NC_000007.12:g.97654422A>G NCBI36
NG_013375.1:g.85290A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+176A>G MANE Select ENSP00000297293.5:n.998+176A>G
ENST00000297293.5:c.998+176A>G ENSP00000297293.5:n.998+176A>G
NM_014916.3:c.998+176A>G NP_055731.2:n.998+176A>G
XM_011515981.1:c.992+176A>G XP_011514283.1:n.992+176A>G
XM_011515981.3:c.992+176A>G XP_011514283.1:n.992+176A>G
NM_014916.4:c.998+176A>G MANE Select NP_055731.2:n.998+176A>G
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