Canonical Allele Identifier: CA4355300
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs372613828
ExAC: 7:97816173 C / T
gnomAD v2: 7-97816173-C-T
gnomAD v3: 7-98186861-C-T
gnomAD v4: 7-98186861-C-T
MyVariant Identifiers: chr7:g.97816173C>T (hg19) chr7:g.98186861C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186861C>T , CM000669.2:g.98186861C>T GRCh38
NC_000007.13:g.97816173C>T , CM000669.1:g.97816173C>T GRCh37
NC_000007.12:g.97654109C>T NCBI36
NG_013375.1:g.84977C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.877-16C>T MANE Select ENSP00000297293.5:n.877-16C>T
ENST00000297293.5:c.877-16C>T ENSP00000297293.5:n.877-16C>T
NM_014916.3:c.877-16C>T NP_055731.2:n.877-16C>T
XM_011515981.1:c.871-16C>T XP_011514283.1:n.871-16C>T
XM_011515981.3:c.871-16C>T XP_011514283.1:n.871-16C>T
NM_014916.4:c.877-16C>T MANE Select NP_055731.2:n.877-16C>T
Search 100 bp 5'
Search 100 bp 3'