Canonical Allele Identifier: CA456635133
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816245A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186933A>T , CM000669.2:g.98186933A>T GRCh38
NC_000007.13:g.97816245A>T , CM000669.1:g.97816245A>T GRCh37
NC_000007.12:g.97654181A>T NCBI36
NG_013375.1:g.85049A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.933A>T MANE Select ENSP00000297293.5:p.Pro311=
ENST00000297293.5:c.933A>T ENSP00000297293.5:p.Pro311=
NM_014916.3:c.933A>T NP_055731.2:p.Pro311=
XM_011515981.1:c.927A>T XP_011514283.1:p.Pro309=
XM_011515981.3:c.927A>T XP_011514283.1:p.Pro309=
NM_014916.4:c.933A>T MANE Select NP_055731.2:p.Pro311=
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Search 100 bp 3'