Canonical Allele Identifier: CA844372559
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1440928949
MyVariant Identifiers: chr7:g.97816579G>C (hg19) chr7:g.98187267G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187267G>C , CM000669.2:g.98187267G>C GRCh38
NC_000007.13:g.97816579G>C , CM000669.1:g.97816579G>C GRCh37
NC_000007.12:g.97654515G>C NCBI36
NG_013375.1:g.85383G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+269G>C MANE Select ENSP00000297293.5:n.998+269G>C
ENST00000297293.5:c.998+269G>C ENSP00000297293.5:n.998+269G>C
NM_014916.3:c.998+269G>C NP_055731.2:n.998+269G>C
XM_011515981.1:c.992+269G>C XP_011514283.1:n.992+269G>C
XM_011515981.3:c.992+269G>C XP_011514283.1:n.992+269G>C
NM_014916.4:c.998+269G>C MANE Select NP_055731.2:n.998+269G>C
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