Canonical Allele Identifier: CA344593588

Gene: LAMB3

Linked Data

• dbSNP Id: rs1473440337
• gnomAD v2: 1-209804017-A-C
• gnomAD v4: 1-209630672-A-C
• MyVariant Identifiers: chr1:g.209804017A>C (hg19) ; chr1:g.209630672A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209630672A>C , CM000663.2:g.209630672A>C	GRCh38
NC_000001.10:g.209804017A>C , CM000663.1:g.209804017A>C	GRCh37
NC_000001.9:g.207870640A>C	NCBI36
NG_007116.1:g.26804T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.886T>G MANE Select	ENSP00000348384.3:p.Phe296Val
ENST00000356082.8:c.886T>G	ENSP00000348384.3:p.Phe296Val
ENST00000367030.7:c.886T>G	ENSP00000355997.3:p.Phe296Val
ENST00000391911.5:c.886T>G	ENSP00000375778.1:p.Phe296Val
NM_000228.2:c.886T>G	NP_000219.2:p.Phe296Val
NM_001017402.1:c.886T>G	NP_001017402.1:p.Phe296Val
NM_001127641.1:c.886T>G	NP_001121113.1:p.Phe296Val
XM_005273124.3:c.886T>G	XP_005273181.1:p.Phe296Val
XM_005273124.4:c.886T>G	XP_005273181.1:p.Phe296Val
XM_017001272.2:c.694T>G	XP_016856761.1:p.Phe232Val
NM_000228.3:c.886T>G MANE Select	NP_000219.2:p.Phe296Val
NM_001017402.2:c.886T>G	NP_001017402.1:p.Phe296Val