Canonical Allele Identifier: CA423032872

Gene: LAMB3

Linked Data

• ClinVar Variation Id: 1112507
• ClinVar RCV Id: RCV001439542
• dbSNP Id: rs1382722706
• gnomAD v3: 1-209634597-G-A
• gnomAD v4: 1-209634597-G-A
• MyVariant Identifiers: chr1:g.209807942G>A (hg19) ; chr1:g.209634597G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209634597G>A , CM000663.2:g.209634597G>A	GRCh38
NC_000001.10:g.209807942G>A , CM000663.1:g.209807942G>A	GRCh37
NC_000001.9:g.207874565G>A	NCBI36
NG_007116.1:g.22879C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.414C>T MANE Select	ENSP00000348384.3:p.Asp138=
ENST00000356082.8:c.414C>T	ENSP00000348384.3:p.Asp138=
ENST00000367030.7:c.414C>T	ENSP00000355997.3:p.Asp138=
ENST00000391911.5:c.414C>T	ENSP00000375778.1:p.Asp138=
ENST00000415782.1:c.414C>T	ENSP00000388960.1:p.Asp138=
NM_000228.2:c.414C>T	NP_000219.2:p.Asp138=
NM_001017402.1:c.414C>T	NP_001017402.1:p.Asp138=
NM_001127641.1:c.414C>T	NP_001121113.1:p.Asp138=
XM_005273124.3:c.414C>T	XP_005273181.1:p.Asp138=
XM_005273124.4:c.414C>T	XP_005273181.1:p.Asp138=
XM_017001272.2:c.373-1464C>T	XP_016856761.1:n.373-1464C>T
NM_000228.3:c.414C>T MANE Select	NP_000219.2:p.Asp138=
NM_001017402.2:c.414C>T	NP_001017402.1:p.Asp138=