Canonical Allele Identifier: CA433634122

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49160276A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122843A>C , CM000665.2:g.49122843A>C	GRCh38
NC_000003.11:g.49160276A>C , CM000665.1:g.49160276A>C	GRCh37
NC_000003.10:g.49135280A>C	NCBI36
NG_008094.1:g.15324T>G
NG_054716.1:g.3096T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4434T>G MANE Select	ENSP00000307156.4:p.Ala1478=
ENST00000305544.8:c.4434T>G	ENSP00000307156.4:p.Ala1478=
ENST00000418109.5:c.4434T>G	ENSP00000388325.1:p.Ala1478=
ENST00000469665.1:n.743T>G
NM_002292.3:c.4434T>G	NP_002283.3:p.Ala1478=
XM_005265127.3:c.4434T>G	XP_005265184.1:p.Ala1478=
XM_005265127.4:c.4434T>G	XP_005265184.1:p.Ala1478=
NM_002292.4:c.4434T>G MANE Select	NP_002283.3:p.Ala1478=