Canonical Allele Identifier: CA730826662

Gene: LAMB3

Linked Data

• dbSNP Id: rs1315070617
• gnomAD v3: 1-209624261-T-TC
• gnomAD v4: 1-209624261-T-TC
• MyVariant Identifiers: chr1:g.209797606_209797607insC (hg19) ; chr1:g.209624261_209624262insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209624266dup , CM000663.2:g.209624266dup	GRCh38
NC_000001.10:g.209797611dup , CM000663.1:g.209797611dup	GRCh37
NC_000001.9:g.207864234dup	NCBI36
NG_007116.1:g.33214dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1977-262dup MANE Select	ENSP00000348384.3:n.1977-262dup
ENST00000356082.8:c.1977-262dup	ENSP00000348384.3:n.1977-262dup
ENST00000367030.7:c.1977-262dup	ENSP00000355997.3:n.1977-262dup
ENST00000391911.5:c.1977-262dup	ENSP00000375778.1:n.1977-262dup
NM_000228.2:c.1977-262dup	NP_000219.2:n.1977-262dup
NM_001017402.1:c.1977-262dup	NP_001017402.1:n.1977-262dup
NM_001127641.1:c.1977-262dup	NP_001121113.1:n.1977-262dup
XM_005273124.3:c.1977-262dup	XP_005273181.1:n.1977-262dup
XM_005273124.4:c.1977-262dup	XP_005273181.1:n.1977-262dup
XM_017001272.2:c.1785-262dup	XP_016856761.1:n.1785-262dup
NM_000228.3:c.1977-262dup MANE Select	NP_000219.2:n.1977-262dup
NM_001017402.2:c.1977-262dup	NP_001017402.1:n.1977-262dup