Canonical Allele Identifier: CA2484302805

Gene: LAMB3

Linked Data

• dbSNP Id: rs1558161143
• gnomAD v4: 1-209634662-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209634662A>C , CM000663.2:g.209634662A>C	GRCh38
NC_000001.10:g.209808007A>C , CM000663.1:g.209808007A>C	GRCh37
NC_000001.9:g.207874630A>C	NCBI36
NG_007116.1:g.22814T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.373-24T>G MANE Select	ENSP00000348384.3:n.373-24T>G
ENST00000356082.8:c.373-24T>G	ENSP00000348384.3:n.373-24T>G
ENST00000367030.7:c.373-24T>G	ENSP00000355997.3:n.373-24T>G
ENST00000391911.5:c.373-24T>G	ENSP00000375778.1:n.373-24T>G
ENST00000415782.1:c.373-24T>G	ENSP00000388960.1:n.373-24T>G
NM_000228.2:c.373-24T>G	NP_000219.2:n.373-24T>G
NM_001017402.1:c.373-24T>G	NP_001017402.1:n.373-24T>G
NM_001127641.1:c.373-24T>G	NP_001121113.1:n.373-24T>G
XM_005273124.3:c.373-24T>G	XP_005273181.1:n.373-24T>G
XM_005273124.4:c.373-24T>G	XP_005273181.1:n.373-24T>G
XM_017001272.2:c.373-1529T>G	XP_016856761.1:n.373-1529T>G
NM_000228.3:c.373-24T>G MANE Select	NP_000219.2:n.373-24T>G
NM_001017402.2:c.373-24T>G	NP_001017402.1:n.373-24T>G