Canonical Allele Identifier: CA344588264

Gene: LAMB3

Linked Data

• ClinVar Variation Id: 1726556
• ClinVar RCV Id: RCV002310240
• MyVariant Identifiers: chr1:g.209796881G>T (hg19) ; chr1:g.209623536G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209623536G>T , CM000663.2:g.209623536G>T	GRCh38
NC_000001.10:g.209796881G>T , CM000663.1:g.209796881G>T	GRCh37
NC_000001.9:g.207863504G>T	NCBI36
NG_007116.1:g.33940C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.2327C>A MANE Select	ENSP00000348384.3:p.Ser776Ter
ENST00000356082.8:c.2327C>A	ENSP00000348384.3:p.Ser776Ter
ENST00000367030.7:c.2327C>A	ENSP00000355997.3:p.Ser776Ter
ENST00000391911.5:c.2327C>A	ENSP00000375778.1:p.Ser776Ter
NM_000228.2:c.2327C>A	NP_000219.2:p.Ser776Ter
NM_001017402.1:c.2327C>A	NP_001017402.1:p.Ser776Ter
NM_001127641.1:c.2327C>A	NP_001121113.1:p.Ser776Ter
XM_005273124.3:c.2327C>A	XP_005273181.1:p.Ser776Ter
XM_005273124.4:c.2327C>A	XP_005273181.1:p.Ser776Ter
XM_017001272.2:c.2135C>A	XP_016856761.1:p.Ser712Ter
NM_000228.3:c.2327C>A MANE Select	NP_000219.2:p.Ser776Ter
NM_001017402.2:c.2327C>A	NP_001017402.1:p.Ser776Ter