Canonical Allele Identifier: CA1375098

Gene: LAMB3

Linked Data

• dbSNP Id: rs752659930
• ExAC: 1:209791942 G / C
• gnomAD v2: 1-209791942-G-C
• MyVariant Identifiers: chr1:g.209791942G>C (hg19) ; chr1:g.209618597G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209618597G>C , CM000663.2:g.209618597G>C	GRCh38
NC_000001.10:g.209791942G>C , CM000663.1:g.209791942G>C	GRCh37
NC_000001.9:g.207858565G>C	NCBI36
NG_007116.1:g.38879C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.2764C>G MANE Select	ENSP00000348384.3:p.Pro922Ala
ENST00000356082.8:c.2764C>G	ENSP00000348384.3:p.Pro922Ala
ENST00000367030.7:c.2764C>G	ENSP00000355997.3:p.Pro922Ala
ENST00000391911.5:c.2764C>G	ENSP00000375778.1:p.Pro922Ala
ENST00000455193.1:c.-30C>G	ENSP00000398683.1:n.-30C>G
NM_000228.2:c.2764C>G	NP_000219.2:p.Pro922Ala
NM_001017402.1:c.2764C>G	NP_001017402.1:p.Pro922Ala
NM_001127641.1:c.2764C>G	NP_001121113.1:p.Pro922Ala
XM_005273124.3:c.2764C>G	XP_005273181.1:p.Pro922Ala
XM_005273124.4:c.2764C>G	XP_005273181.1:p.Pro922Ala
XM_017001272.2:c.2572C>G	XP_016856761.1:p.Pro858Ala
NM_000228.3:c.2764C>G MANE Select	NP_000219.2:p.Pro922Ala
NM_001017402.2:c.2764C>G	NP_001017402.1:p.Pro922Ala