Canonical Allele Identifier: CA1375562

Gene: LAMB3

Linked Data

• dbSNP Id: rs770003713
• ExAC: 1:209800316 C / A
• gnomAD v2: 1-209800316-C-A
• gnomAD v3: 1-209626971-C-A
• gnomAD v4: 1-209626971-C-A
• MyVariant Identifiers: chr1:g.209800316C>A (hg19) ; chr1:g.209626971C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209626971C>A , CM000663.2:g.209626971C>A	GRCh38
NC_000001.10:g.209800316C>A , CM000663.1:g.209800316C>A	GRCh37
NC_000001.9:g.207866939C>A	NCBI36
NG_007116.1:g.30505G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1493G>T MANE Select	ENSP00000348384.3:p.Gly498Val
ENST00000356082.8:c.1493G>T	ENSP00000348384.3:p.Gly498Val
ENST00000367030.7:c.1493G>T	ENSP00000355997.3:p.Gly498Val
ENST00000391911.5:c.1493G>T	ENSP00000375778.1:p.Gly498Val
NM_000228.2:c.1493G>T	NP_000219.2:p.Gly498Val
NM_001017402.1:c.1493G>T	NP_001017402.1:p.Gly498Val
NM_001127641.1:c.1493G>T	NP_001121113.1:p.Gly498Val
XM_005273124.3:c.1493G>T	XP_005273181.1:p.Gly498Val
XM_005273124.4:c.1493G>T	XP_005273181.1:p.Gly498Val
XM_017001272.2:c.1301G>T	XP_016856761.1:p.Gly434Val
NM_000228.3:c.1493G>T MANE Select	NP_000219.2:p.Gly498Val
NM_001017402.2:c.1493G>T	NP_001017402.1:p.Gly498Val