Canonical Allele Identifier: CA423142449

Gene: LAMB3

Linked Data

• ClinVar Variation Id: 2854991
• ClinVar RCV Id: RCV003699211
• dbSNP Id: rs774502087
• MyVariant Identifiers: chr1:g.209797285C>A (hg19) ; chr1:g.209623940C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209623940C>A , CM000663.2:g.209623940C>A	GRCh38
NC_000001.10:g.209797285C>A , CM000663.1:g.209797285C>A	GRCh37
NC_000001.9:g.207863908C>A	NCBI36
NG_007116.1:g.33536G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.2037G>T MANE Select	ENSP00000348384.3:p.Pro679=
ENST00000356082.8:c.2037G>T	ENSP00000348384.3:p.Pro679=
ENST00000367030.7:c.2037G>T	ENSP00000355997.3:p.Pro679=
ENST00000391911.5:c.2037G>T	ENSP00000375778.1:p.Pro679=
NM_000228.2:c.2037G>T	NP_000219.2:p.Pro679=
NM_001017402.1:c.2037G>T	NP_001017402.1:p.Pro679=
NM_001127641.1:c.2037G>T	NP_001121113.1:p.Pro679=
XM_005273124.3:c.2037G>T	XP_005273181.1:p.Pro679=
XM_005273124.4:c.2037G>T	XP_005273181.1:p.Pro679=
XM_017001272.2:c.1845G>T	XP_016856761.1:p.Pro615=
NM_000228.3:c.2037G>T MANE Select	NP_000219.2:p.Pro679=
NM_001017402.2:c.2037G>T	NP_001017402.1:p.Pro679=