Canonical Allele Identifier: CA344592134

Gene: LAMB3

Linked Data

• MyVariant Identifiers: chr1:g.209803084A>G (hg19) ; chr1:g.209629739A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209629739A>G , CM000663.2:g.209629739A>G	GRCh38
NC_000001.10:g.209803084A>G , CM000663.1:g.209803084A>G	GRCh37
NC_000001.9:g.207869707A>G	NCBI36
NG_007116.1:g.27737T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.1130T>C MANE Select	ENSP00000348384.3:p.Ile377Thr
ENST00000356082.8:c.1130T>C	ENSP00000348384.3:p.Ile377Thr
ENST00000367030.7:c.1130T>C	ENSP00000355997.3:p.Ile377Thr
ENST00000391911.5:c.1130T>C	ENSP00000375778.1:p.Ile377Thr
NM_000228.2:c.1130T>C	NP_000219.2:p.Ile377Thr
NM_001017402.1:c.1130T>C	NP_001017402.1:p.Ile377Thr
NM_001127641.1:c.1130T>C	NP_001121113.1:p.Ile377Thr
XM_005273124.3:c.1130T>C	XP_005273181.1:p.Ile377Thr
XM_005273124.4:c.1130T>C	XP_005273181.1:p.Ile377Thr
XM_017001272.2:c.938T>C	XP_016856761.1:p.Ile313Thr
NM_000228.3:c.1130T>C MANE Select	NP_000219.2:p.Ile377Thr
NM_001017402.2:c.1130T>C	NP_001017402.1:p.Ile377Thr