Canonical Allele Identifier: CA344597507

Gene: LAMB3

Linked Data

• MyVariant Identifiers: chr1:g.209811877A>T (hg19) ; chr1:g.209638532A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209638532A>T , CM000663.2:g.209638532A>T	GRCh38
NC_000001.10:g.209811877A>T , CM000663.1:g.209811877A>T	GRCh37
NC_000001.9:g.207878500A>T	NCBI36
NG_007116.1:g.18944T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.298+2T>A MANE Select	ENSP00000348384.3:n.298+2T>A
ENST00000356082.8:c.298+2T>A	ENSP00000348384.3:n.298+2T>A
ENST00000367030.7:c.298+2T>A	ENSP00000355997.3:n.298+2T>A
ENST00000391911.5:c.298+2T>A	ENSP00000375778.1:n.298+2T>A
ENST00000415782.1:c.298+2T>A	ENSP00000388960.1:n.298+2T>A
NM_000228.2:c.298+2T>A	NP_000219.2:n.298+2T>A
NM_001017402.1:c.298+2T>A	NP_001017402.1:n.298+2T>A
NM_001127641.1:c.298+2T>A	NP_001121113.1:n.298+2T>A
XM_005273124.3:c.298+2T>A	XP_005273181.1:n.298+2T>A
XM_005273124.4:c.298+2T>A	XP_005273181.1:n.298+2T>A
XM_017001272.2:c.298+2T>A	XP_016856761.1:n.298+2T>A
NM_000228.3:c.298+2T>A MANE Select	NP_000219.2:n.298+2T>A
NM_001017402.2:c.298+2T>A	NP_001017402.1:n.298+2T>A