Canonical Allele Identifier: CA74480580

Gene: LAMB2

Linked Data

• dbSNP Id: rs1041906247
• MyVariant Identifiers: chr3:g.49162638G>T (hg19) ; chr3:g.49125205G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125205G>T , CM000665.2:g.49125205G>T	GRCh38
NC_000003.11:g.49162638G>T , CM000665.1:g.49162638G>T	GRCh37
NC_000003.10:g.49137642G>T	NCBI36
NG_008094.1:g.12962C>A
NG_054716.1:g.734C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2721-36C>A MANE Select	ENSP00000307156.4:n.2721-36C>A
ENST00000305544.8:c.2721-36C>A	ENSP00000307156.4:n.2721-36C>A
ENST00000418109.5:c.2721-36C>A	ENSP00000388325.1:n.2721-36C>A
ENST00000462930.5:n.128-36C>A
ENST00000464891.5:n.454-36C>A
ENST00000483057.1:n.321-36C>A
ENST00000486298.5:n.426-36C>A
NM_002292.3:c.2721-36C>A	NP_002283.3:n.2721-36C>A
XM_005265127.3:c.2721-36C>A	XP_005265184.1:n.2721-36C>A
XM_005265127.4:c.2721-36C>A	XP_005265184.1:n.2721-36C>A
NM_002292.4:c.2721-36C>A MANE Select	NP_002283.3:n.2721-36C>A