Canonical Allele Identifier: CA456635155
Gene: LMTK2 HGNC NCBI

Linked Data

gnomAD v4: 7-98186936-A-G
MyVariant Identifiers: chr7:g.97816248A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186936A>G , CM000669.2:g.98186936A>G GRCh38
NC_000007.13:g.97816248A>G , CM000669.1:g.97816248A>G GRCh37
NC_000007.12:g.97654184A>G NCBI36
NG_013375.1:g.85052A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.936A>G MANE Select ENSP00000297293.5:p.Glu312=
ENST00000297293.5:c.936A>G ENSP00000297293.5:p.Glu312=
NM_014916.3:c.936A>G NP_055731.2:p.Glu312=
XM_011515981.1:c.930A>G XP_011514283.1:p.Glu310=
XM_011515981.3:c.930A>G XP_011514283.1:p.Glu310=
NM_014916.4:c.936A>G MANE Select NP_055731.2:p.Glu312=
Search 100 bp 5'
Search 100 bp 3'