Canonical Allele Identifier: CA9611629
Gene: LIM2 HGNC NCBI
LIM2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 329977
ClinVar RCV Id: RCV000319552
dbSNP Id: rs760441995
ExAC: 19:51890590 G / A
gnomAD v2: 19-51890590-G-A
gnomAD v3: 19-51387336-G-A
gnomAD v4: 19-51387336-G-A
MyVariant Identifiers: chr19:g.51890590G>A (hg19) chr19:g.51387336G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51387336G>A , CM000681.2:g.51387336G>A GRCh38
NC_000019.9:g.51890590G>A , CM000681.1:g.51890590G>A GRCh37
NC_000019.8:g.56582402G>A NCBI36
NG_012924.1:g.5621C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000596399.2:c.108C>T (LIM2) MANE Select ENSP00000472090.2:p.Ser36=
ENST00000221973.7:c.108C>T (LIM2) ENSP00000221973.2:p.Ser36=
ENST00000596399.1:c.108C>T (LIM2) ENSP00000472090.1:p.Ser36=
NM_001161748.1:c.108C>T (LIM2) NP_001155220.1:p.Ser36=
NM_030657.3:c.108C>T (LIM2) NP_085915.2:p.Ser36=
XR_002958395.1:n.414G>A (LIM2-AS1)
XR_002958396.1:n.414G>A (LIM2-AS1)
XR_002958397.1:n.414G>A (LIM2-AS1)
XR_002958398.1:n.414G>A (LIM2-AS1)
NM_001161748.2:c.108C>T (LIM2) MANE Select NP_001155220.1:p.Ser36=
NM_030657.4:c.108C>T (LIM2) NP_085915.2:p.Ser36=
Search 100 bp 5'
Search 100 bp 3'