Canonical Allele Identifier: CA344594814

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209632759-T-C
• MyVariant Identifiers: chr1:g.209806104T>C (hg19) ; chr1:g.209632759T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209632759T>C , CM000663.2:g.209632759T>C	GRCh38
NC_000001.10:g.209806104T>C , CM000663.1:g.209806104T>C	GRCh37
NC_000001.9:g.207872727T>C	NCBI36
NG_007116.1:g.24717A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.646A>G MANE Select	ENSP00000348384.3:p.Asn216Asp
ENST00000356082.8:c.646A>G	ENSP00000348384.3:p.Asn216Asp
ENST00000367030.7:c.646A>G	ENSP00000355997.3:p.Asn216Asp
ENST00000391911.5:c.646A>G	ENSP00000375778.1:p.Asn216Asp
NM_000228.2:c.646A>G	NP_000219.2:p.Asn216Asp
NM_001017402.1:c.646A>G	NP_001017402.1:p.Asn216Asp
NM_001127641.1:c.646A>G	NP_001121113.1:p.Asn216Asp
XM_005273124.3:c.646A>G	XP_005273181.1:p.Asn216Asp
XM_005273124.4:c.646A>G	XP_005273181.1:p.Asn216Asp
XM_017001272.2:c.454A>G	XP_016856761.1:p.Asn152Asp
NM_000228.3:c.646A>G MANE Select	NP_000219.2:p.Asn216Asp
NM_001017402.2:c.646A>G	NP_001017402.1:p.Asn216Asp