Canonical Allele Identifier: CA403255329
Community Standard Title: NM_032737.4(LMNB2):c.750G>T (p.Gln250His)
Gene: LMNB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2435106C>A , CM000681.2:g.2435106C>A GRCh38
NC_000019.9:g.2435104C>A , CM000681.1:g.2435104C>A GRCh37
NC_000019.8:g.2386104C>A NCBI36
NG_008355.1:g.26855G>T

Transcript Alleles

HGVS Amino-acid Change
NM_032737.4:c.750G>T MANE Select NP_116126.3:p.Gln250His
ENST00000325327.4:c.750G>T MANE Select ENSP00000327054.3:p.Gln250His
NM_032737.3:c.750G>T NP_116126.3:p.Gln250His
ENST00000325327.3:c.750G>T ENSP00000327054.3:p.Gln250His
ENST00000527409.1:n.386G>T
ENST00000534495.1:n.388G>T
XM_011528378.1:c.750G>T XP_011526680.1:p.Gln250His
XM_011528379.1:c.402G>T XP_011526681.1:p.Gln134His