Canonical Allele Identifier: CA352717432

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49162588A>G (hg19) ; chr3:g.49125155A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125155A>G , CM000665.2:g.49125155A>G	GRCh38
NC_000003.11:g.49162588A>G , CM000665.1:g.49162588A>G	GRCh37
NC_000003.10:g.49137592A>G	NCBI36
NG_008094.1:g.13012T>C
NG_054716.1:g.784T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000305544.9:c.2735T>C MANE Select	ENSP00000307156.4:p.Phe912Ser
ENST00000305544.8:c.2735T>C	ENSP00000307156.4:p.Phe912Ser
ENST00000418109.5:c.2735T>C	ENSP00000388325.1:p.Phe912Ser
ENST00000462930.5:n.142T>C
ENST00000464891.5:n.468T>C
ENST00000483057.1:n.335T>C
ENST00000486298.5:n.440T>C
ENST00000542580.1:n.50T>C
NM_002292.3:c.2735T>C	NP_002283.3:p.Phe912Ser
XM_005265127.3:c.2735T>C	XP_005265184.1:p.Phe912Ser
XM_005265127.4:c.2735T>C	XP_005265184.1:p.Phe912Ser
NM_002292.4:c.2735T>C MANE Select	NP_002283.3:p.Phe912Ser