Canonical Allele Identifier: CA36760869

Gene: LAMB3

Linked Data

• dbSNP Id: rs376089536
• gnomAD v2: 1-209806665-C-CGT
• gnomAD v3: 1-209633320-C-CGT
• gnomAD v4: 1-209633320-C-CGT
• MyVariant Identifiers: chr1:g.209806667_209806668insGT (hg19) ; chr1:g.209806665_209806666insGT (hg19) ; chr1:g.209633322_209633323insGT (hg38) ; chr1:g.209633320_209633321insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209633333_209633334dup , CM000663.2:g.209633333_209633334dup	GRCh38
NC_000001.10:g.209806678_209806679dup , CM000663.1:g.209806678_209806679dup	GRCh37
NC_000001.9:g.207873301_207873302dup	NCBI36
NG_007116.1:g.24154_24155dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.565-189_565-188dup MANE Select	ENSP00000348384.3:n.565-189_565-188dup
ENST00000356082.8:c.565-189_565-188dup	ENSP00000348384.3:n.565-189_565-188dup
ENST00000367030.7:c.565-189_565-188dup	ENSP00000355997.3:n.565-189_565-188dup
ENST00000391911.5:c.565-189_565-188dup	ENSP00000375778.1:n.565-189_565-188dup
NM_000228.2:c.565-189_565-188dup	NP_000219.2:n.565-189_565-188dup
NM_001017402.1:c.565-189_565-188dup	NP_001017402.1:n.565-189_565-188dup
NM_001127641.1:c.565-189_565-188dup	NP_001121113.1:n.565-189_565-188dup
XM_005273124.3:c.565-189_565-188dup	XP_005273181.1:n.565-189_565-188dup
XM_005273124.4:c.565-189_565-188dup	XP_005273181.1:n.565-189_565-188dup
XM_017001272.2:c.373-189_373-188dup	XP_016856761.1:n.373-189_373-188dup
NM_000228.3:c.565-189_565-188dup MANE Select	NP_000219.2:n.565-189_565-188dup
NM_001017402.2:c.565-189_565-188dup	NP_001017402.1:n.565-189_565-188dup