Canonical Allele Identifier: CA2393566

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49121389G>C , CM000665.2:g.49121389G>C	GRCh38
NC_000003.11:g.49158822G>C , CM000665.1:g.49158822G>C	GRCh37
NC_000003.10:g.49133826G>C	NCBI36
NG_008094.1:g.16778C>G
NG_054716.1:g.4550C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002292.4:c.5261-27C>G MANE Select	NP_002283.3:n.5261-27C>G
ENST00000305544.9:c.5261-27C>G MANE Select	ENSP00000307156.4:n.5261-27C>G
NM_002292.3:c.5261-27C>G	NP_002283.3:n.5261-27C>G
ENST00000305544.8:c.5261-27C>G	ENSP00000307156.4:n.5261-27C>G
ENST00000418109.5:c.5261-27C>G	ENSP00000388325.1:n.5261-27C>G
ENST00000467506.5:n.414C>G
ENST00000484713.1:n.165-27C>G
ENST00000498377.1:n.916-27C>G
XM_005265127.3:c.5261-27C>G	XP_005265184.1:n.5261-27C>G
XM_005265127.4:c.5261-27C>G	XP_005265184.1:n.5261-27C>G