Canonical Allele Identifier: CA456635177
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816251A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186939A>G , CM000669.2:g.98186939A>G GRCh38
NC_000007.13:g.97816251A>G , CM000669.1:g.97816251A>G GRCh37
NC_000007.12:g.97654187A>G NCBI36
NG_013375.1:g.85055A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297293.6:c.939A>G MANE Select ENSP00000297293.5:p.Leu313=
ENST00000297293.5:c.939A>G ENSP00000297293.5:p.Leu313=
NM_014916.3:c.939A>G NP_055731.2:p.Leu313=
XM_011515981.1:c.933A>G XP_011514283.1:p.Leu311=
XM_011515981.3:c.933A>G XP_011514283.1:p.Leu311=
NM_014916.4:c.939A>G MANE Select NP_055731.2:p.Leu313=
Search 100 bp 5'
Search 100 bp 3'