Canonical Allele Identifier: CA9611622
Gene: LIM2 HGNC NCBI
LIM2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51387313C>T , CM000681.2:g.51387313C>T GRCh38
NC_000019.9:g.51890567C>T , CM000681.1:g.51890567C>T GRCh37
NC_000019.8:g.56582379C>T NCBI36
NG_012924.1:g.5644G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000596399.2:c.131G>A (LIM2) MANE Select ENSP00000472090.2:p.Arg44Gln
ENST00000221973.7:c.131G>A (LIM2) ENSP00000221973.2:p.Arg44Gln
ENST00000596399.1:c.131G>A (LIM2) ENSP00000472090.1:p.Arg44Gln
NM_001161748.1:c.131G>A (LIM2) NP_001155220.1:p.Arg44Gln
NM_030657.3:c.131G>A (LIM2) NP_085915.2:p.Arg44Gln
XR_002958395.1:n.391C>T (LIM2-AS1)
XR_002958396.1:n.391C>T (LIM2-AS1)
XR_002958397.1:n.391C>T (LIM2-AS1)
XR_002958398.1:n.391C>T (LIM2-AS1)
NM_001161748.2:c.131G>A (LIM2) MANE Select NP_001155220.1:p.Arg44Gln
NM_030657.4:c.131G>A (LIM2) NP_085915.2:p.Arg44Gln