Canonical Allele Identifier: CA344566199

Gene: LAMB3

Linked Data

• MyVariant Identifiers: chr1:g.209823352C>T (hg19) ; chr1:g.209650007C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209650007C>T , CM000663.2:g.209650007C>T	GRCh38
NC_000001.10:g.209823352C>T , CM000663.1:g.209823352C>T	GRCh37
NC_000001.9:g.207889975C>T	NCBI36
NG_007116.1:g.7469G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.140G>A MANE Select	ENSP00000348384.3:p.Cys47Tyr
ENST00000356082.8:c.140G>A	ENSP00000348384.3:p.Cys47Tyr
ENST00000367030.7:c.140G>A	ENSP00000355997.3:p.Cys47Tyr
ENST00000391911.5:c.140G>A	ENSP00000375778.1:p.Cys47Tyr
ENST00000415782.1:c.140G>A	ENSP00000388960.1:p.Cys47Tyr
NM_000228.2:c.140G>A	NP_000219.2:p.Cys47Tyr
NM_001017402.1:c.140G>A	NP_001017402.1:p.Cys47Tyr
NM_001127641.1:c.140G>A	NP_001121113.1:p.Cys47Tyr
XM_005273124.3:c.140G>A	XP_005273181.1:p.Cys47Tyr
XM_005273124.4:c.140G>A	XP_005273181.1:p.Cys47Tyr
XM_017001272.2:c.140G>A	XP_016856761.1:p.Cys47Tyr
NM_000228.3:c.140G>A MANE Select	NP_000219.2:p.Cys47Tyr
NM_001017402.2:c.140G>A	NP_001017402.1:p.Cys47Tyr