Canonical Allele Identifier: CA423032293
Gene: LAMB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.209803194T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209629849T>C , CM000663.2:g.209629849T>C GRCh38
NC_000001.10:g.209803194T>C , CM000663.1:g.209803194T>C GRCh37
NC_000001.9:g.207869817T>C NCBI36
NG_007116.1:g.27627A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.1020A>G MANE Select ENSP00000348384.3:p.Gly340=
ENST00000356082.8:c.1020A>G ENSP00000348384.3:p.Gly340=
ENST00000367030.7:c.1020A>G ENSP00000355997.3:p.Gly340=
ENST00000391911.5:c.1020A>G ENSP00000375778.1:p.Gly340=
NM_000228.2:c.1020A>G NP_000219.2:p.Gly340=
NM_001017402.1:c.1020A>G NP_001017402.1:p.Gly340=
NM_001127641.1:c.1020A>G NP_001121113.1:p.Gly340=
XM_005273124.3:c.1020A>G XP_005273181.1:p.Gly340=
XM_005273124.4:c.1020A>G XP_005273181.1:p.Gly340=
XM_017001272.2:c.828A>G XP_016856761.1:p.Gly276=
NM_000228.3:c.1020A>G MANE Select NP_000219.2:p.Gly340=
NM_001017402.2:c.1020A>G NP_001017402.1:p.Gly340=