Canonical Allele Identifier: CA4355297

Gene: LMTK2

Linked Data

• dbSNP Id: rs757539164
• ExAC: 7:97816152 T / C
• gnomAD v2: 7-97816152-T-C
• gnomAD v4: 7-98186840-T-C
• MyVariant Identifiers: chr7:g.97816152T>C (hg19) ; chr7:g.98186840T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98186840T>C , CM000669.2:g.98186840T>C	GRCh38
NC_000007.13:g.97816152T>C , CM000669.1:g.97816152T>C	GRCh37
NC_000007.12:g.97654088T>C	NCBI36
NG_013375.1:g.84956T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.877-37T>C MANE Select	ENSP00000297293.5:n.877-37T>C
ENST00000297293.5:c.877-37T>C	ENSP00000297293.5:n.877-37T>C
NM_014916.3:c.877-37T>C	NP_055731.2:n.877-37T>C
XM_011515981.1:c.871-37T>C	XP_011514283.1:n.871-37T>C
XM_011515981.3:c.871-37T>C	XP_011514283.1:n.871-37T>C
NM_014916.4:c.877-37T>C MANE Select	NP_055731.2:n.877-37T>C