Canonical Allele Identifier: CA352714762

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49162308G>C (hg19) ; chr3:g.49124875G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49124875G>C , CM000665.2:g.49124875G>C	GRCh38
NC_000003.11:g.49162308G>C , CM000665.1:g.49162308G>C	GRCh37
NC_000003.10:g.49137312G>C	NCBI36
NG_008094.1:g.13292C>G
NG_054716.1:g.1064C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2935C>G MANE Select	ENSP00000307156.4:p.Pro979Ala
ENST00000305544.8:c.2935C>G	ENSP00000307156.4:p.Pro979Ala
ENST00000418109.5:c.2935C>G	ENSP00000388325.1:p.Pro979Ala
ENST00000462930.5:n.342C>G
ENST00000464891.5:n.668C>G
ENST00000483057.1:n.535C>G
ENST00000542580.1:n.250C>G
NM_002292.3:c.2935C>G	NP_002283.3:p.Pro979Ala
XM_005265127.3:c.2935C>G	XP_005265184.1:p.Pro979Ala
XM_005265127.4:c.2935C>G	XP_005265184.1:p.Pro979Ala
NM_002292.4:c.2935C>G MANE Select	NP_002283.3:p.Pro979Ala