Canonical Allele Identifier: CA844372557
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1346787437
gnomAD v3: 7-98187253-G-A
gnomAD v4: 7-98187253-G-A
MyVariant Identifiers: chr7:g.97816565G>A (hg19) chr7:g.98187253G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187253G>A , CM000669.2:g.98187253G>A GRCh38
NC_000007.13:g.97816565G>A , CM000669.1:g.97816565G>A GRCh37
NC_000007.12:g.97654501G>A NCBI36
NG_013375.1:g.85369G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+255G>A MANE Select ENSP00000297293.5:n.998+255G>A
ENST00000297293.5:c.998+255G>A ENSP00000297293.5:n.998+255G>A
NM_014916.3:c.998+255G>A NP_055731.2:n.998+255G>A
XM_011515981.1:c.992+255G>A XP_011514283.1:n.992+255G>A
XM_011515981.3:c.992+255G>A XP_011514283.1:n.992+255G>A
NM_014916.4:c.998+255G>A MANE Select NP_055731.2:n.998+255G>A
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