Canonical Allele Identifier: CA456635107
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816242T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186930T>C , CM000669.2:g.98186930T>C GRCh38
NC_000007.13:g.97816242T>C , CM000669.1:g.97816242T>C GRCh37
NC_000007.12:g.97654178T>C NCBI36
NG_013375.1:g.85046T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297293.6:c.930T>C MANE Select ENSP00000297293.5:p.Ala310=
ENST00000297293.5:c.930T>C ENSP00000297293.5:p.Ala310=
NM_014916.3:c.930T>C NP_055731.2:p.Ala310=
XM_011515981.1:c.924T>C XP_011514283.1:p.Ala308=
XM_011515981.3:c.924T>C XP_011514283.1:p.Ala308=
NM_014916.4:c.930T>C MANE Select NP_055731.2:p.Ala310=
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