Canonical Allele Identifier: CA74489576

Gene: LAMB2

Linked Data

• dbSNP Id: rs544110245
• MyVariant Identifiers: chr3:g.49169396G>A (hg19) ; chr3:g.49131963G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49131963G>A , CM000665.2:g.49131963G>A	GRCh38
NC_000003.11:g.49169396G>A , CM000665.1:g.49169396G>A	GRCh37
NC_000003.10:g.49144400G>A	NCBI36
NG_008094.1:g.6204C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.459+153C>T MANE Select	ENSP00000307156.4:n.459+153C>T
ENST00000305544.8:c.459+153C>T	ENSP00000307156.4:n.459+153C>T
ENST00000418109.5:c.459+153C>T	ENSP00000388325.1:n.459+153C>T
ENST00000494831.1:c.12+153C>T	ENSP00000444751.1:n.12+153C>T
NM_002292.3:c.459+153C>T	NP_002283.3:n.459+153C>T
XM_005265127.3:c.459+153C>T	XP_005265184.1:n.459+153C>T
XM_005265127.4:c.459+153C>T	XP_005265184.1:n.459+153C>T
NM_002292.4:c.459+153C>T MANE Select	NP_002283.3:n.459+153C>T