Canonical Allele Identifier: CA4355311
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs377439511
ExAC: 7:97816249 T / C
gnomAD v2: 7-97816249-T-C
gnomAD v4: 7-98186937-T-C
MyVariant Identifiers: chr7:g.97816249T>C (hg19) chr7:g.98186937T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186937T>C , CM000669.2:g.98186937T>C GRCh38
NC_000007.13:g.97816249T>C , CM000669.1:g.97816249T>C GRCh37
NC_000007.12:g.97654185T>C NCBI36
NG_013375.1:g.85053T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297293.6:c.937T>C MANE Select ENSP00000297293.5:p.Leu313=
ENST00000297293.5:c.937T>C ENSP00000297293.5:p.Leu313=
NM_014916.3:c.937T>C NP_055731.2:p.Leu313=
XM_011515981.1:c.931T>C XP_011514283.1:p.Leu311=
XM_011515981.3:c.931T>C XP_011514283.1:p.Leu311=
NM_014916.4:c.937T>C MANE Select NP_055731.2:p.Leu313=
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