Canonical Allele Identifier: CA2394146
Community Standard Title: NM_002292.4(LAMB2):c.2975T>C (p.Ile992Thr)
Gene: LAMB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49124835A>G , CM000665.2:g.49124835A>G GRCh38
NC_000003.11:g.49162268A>G , CM000665.1:g.49162268A>G GRCh37
NC_000003.10:g.49137272A>G NCBI36
NG_008094.1:g.13332T>C
NG_054716.1:g.1104T>C

Transcript Alleles

HGVS Amino-acid Change
NM_002292.4:c.2975T>C MANE Select NP_002283.3:p.Ile992Thr
ENST00000305544.9:c.2975T>C MANE Select ENSP00000307156.4:p.Ile992Thr
NM_002292.3:c.2975T>C NP_002283.3:p.Ile992Thr
ENST00000305544.8:c.2975T>C ENSP00000307156.4:p.Ile992Thr
ENST00000418109.5:c.2975T>C ENSP00000388325.1:p.Ile992Thr
ENST00000462930.5:n.382T>C
ENST00000464891.5:n.708T>C
ENST00000542580.1:n.290T>C
XM_005265127.3:c.2975T>C XP_005265184.1:p.Ile992Thr
XM_005265127.4:c.2975T>C XP_005265184.1:p.Ile992Thr