Canonical Allele Identifier: CA344585267

Gene: LAMB3

Linked Data

• dbSNP Id: rs1307953034
• gnomAD v3: 1-209618609-C-T
• gnomAD v4: 1-209618609-C-T
• MyVariant Identifiers: chr1:g.209791954C>T (hg19) ; chr1:g.209618609C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209618609C>T , CM000663.2:g.209618609C>T	GRCh38
NC_000001.10:g.209791954C>T , CM000663.1:g.209791954C>T	GRCh37
NC_000001.9:g.207858577C>T	NCBI36
NG_007116.1:g.38867G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.2752G>A MANE Select	ENSP00000348384.3:p.Ala918Thr
ENST00000356082.8:c.2752G>A	ENSP00000348384.3:p.Ala918Thr
ENST00000367030.7:c.2752G>A	ENSP00000355997.3:p.Ala918Thr
ENST00000391911.5:c.2752G>A	ENSP00000375778.1:p.Ala918Thr
ENST00000455193.1:c.-42G>A	ENSP00000398683.1:n.-42G>A
NM_000228.2:c.2752G>A	NP_000219.2:p.Ala918Thr
NM_001017402.1:c.2752G>A	NP_001017402.1:p.Ala918Thr
NM_001127641.1:c.2752G>A	NP_001121113.1:p.Ala918Thr
XM_005273124.3:c.2752G>A	XP_005273181.1:p.Ala918Thr
XM_005273124.4:c.2752G>A	XP_005273181.1:p.Ala918Thr
XM_017001272.2:c.2560G>A	XP_016856761.1:p.Ala854Thr
NM_000228.3:c.2752G>A MANE Select	NP_000219.2:p.Ala918Thr
NM_001017402.2:c.2752G>A	NP_001017402.1:p.Ala918Thr