Canonical Allele Identifier: CA352693793

Gene: LAMB2

Linked Data

• dbSNP Id: rs2045364394
• MyVariant Identifiers: chr3:g.49160352A>G (hg19) ; chr3:g.49122919A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122919A>G , CM000665.2:g.49122919A>G	GRCh38
NC_000003.11:g.49160352A>G , CM000665.1:g.49160352A>G	GRCh37
NC_000003.10:g.49135356A>G	NCBI36
NG_008094.1:g.15248T>C
NG_054716.1:g.3020T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4358T>C MANE Select	ENSP00000307156.4:p.Leu1453Pro
ENST00000305544.8:c.4358T>C	ENSP00000307156.4:p.Leu1453Pro
ENST00000418109.5:c.4358T>C	ENSP00000388325.1:p.Leu1453Pro
ENST00000469665.1:n.667T>C
NM_002292.3:c.4358T>C	NP_002283.3:p.Leu1453Pro
XM_005265127.3:c.4358T>C	XP_005265184.1:p.Leu1453Pro
XM_005265127.4:c.4358T>C	XP_005265184.1:p.Leu1453Pro
NM_002292.4:c.4358T>C MANE Select	NP_002283.3:p.Leu1453Pro