Canonical Allele Identifier: CA576377439
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1218153660
gnomAD v2: 7-97816569-C-G
gnomAD v3: 7-98187257-C-G
gnomAD v4: 7-98187257-C-G
MyVariant Identifiers: chr7:g.97816569C>G (hg19) chr7:g.98187257C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187257C>G , CM000669.2:g.98187257C>G GRCh38
NC_000007.13:g.97816569C>G , CM000669.1:g.97816569C>G GRCh37
NC_000007.12:g.97654505C>G NCBI36
NG_013375.1:g.85373C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+259C>G MANE Select ENSP00000297293.5:n.998+259C>G
ENST00000297293.5:c.998+259C>G ENSP00000297293.5:n.998+259C>G
NM_014916.3:c.998+259C>G NP_055731.2:n.998+259C>G
XM_011515981.1:c.992+259C>G XP_011514283.1:n.992+259C>G
XM_011515981.3:c.992+259C>G XP_011514283.1:n.992+259C>G
NM_014916.4:c.998+259C>G MANE Select NP_055731.2:n.998+259C>G
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