Canonical Allele Identifier: CA344584477

Gene: LAMB3

Linked Data

• ClinVar Variation Id: 983935
• ClinVar RCV Id: RCV001263939
• dbSNP Id: rs1666017894
• MyVariant Identifiers: chr1:g.209790928G>A (hg19) ; chr1:g.209617583G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209617583G>A , CM000663.2:g.209617583G>A	GRCh38
NC_000001.10:g.209790928G>A , CM000663.1:g.209790928G>A	GRCh37
NC_000001.9:g.207857551G>A	NCBI36
NG_007116.1:g.39893C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.3055C>T MANE Select	ENSP00000348384.3:p.Gln1019Ter
ENST00000356082.8:c.3055C>T	ENSP00000348384.3:p.Gln1019Ter
ENST00000367030.7:c.3055C>T	ENSP00000355997.3:p.Gln1019Ter
ENST00000391911.5:c.3055C>T	ENSP00000375778.1:p.Gln1019Ter
ENST00000455193.1:c.262C>T	ENSP00000398683.1:p.Gln88Ter
NM_000228.2:c.3055C>T	NP_000219.2:p.Gln1019Ter
NM_001017402.1:c.3055C>T	NP_001017402.1:p.Gln1019Ter
NM_001127641.1:c.3055C>T	NP_001121113.1:p.Gln1019Ter
XM_005273124.3:c.3055C>T	XP_005273181.1:p.Gln1019Ter
XM_005273124.4:c.3055C>T	XP_005273181.1:p.Gln1019Ter
XM_017001272.2:c.2863C>T	XP_016856761.1:p.Gln955Ter
NM_000228.3:c.3055C>T MANE Select	NP_000219.2:p.Gln1019Ter
NM_001017402.2:c.3055C>T	NP_001017402.1:p.Gln1019Ter