Canonical Allele Identifier: CA344566317

Gene: LAMB3

Linked Data

• dbSNP Id: rs2076552086
• gnomAD v3: 1-209650070-C-G
• gnomAD v4: 1-209650070-C-G
• MyVariant Identifiers: chr1:g.209823415C>G (hg19) ; chr1:g.209650070C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209650070C>G , CM000663.2:g.209650070C>G	GRCh38
NC_000001.10:g.209823415C>G , CM000663.1:g.209823415C>G	GRCh37
NC_000001.9:g.207890038C>G	NCBI36
NG_007116.1:g.7406G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.77G>C MANE Select	ENSP00000348384.3:p.Cys26Ser
ENST00000356082.8:c.77G>C	ENSP00000348384.3:p.Cys26Ser
ENST00000367030.7:c.77G>C	ENSP00000355997.3:p.Cys26Ser
ENST00000391911.5:c.77G>C	ENSP00000375778.1:p.Cys26Ser
ENST00000415782.1:c.77G>C	ENSP00000388960.1:p.Cys26Ser
NM_000228.2:c.77G>C	NP_000219.2:p.Cys26Ser
NM_001017402.1:c.77G>C	NP_001017402.1:p.Cys26Ser
NM_001127641.1:c.77G>C	NP_001121113.1:p.Cys26Ser
XM_005273124.3:c.77G>C	XP_005273181.1:p.Cys26Ser
XM_005273124.4:c.77G>C	XP_005273181.1:p.Cys26Ser
XM_017001272.2:c.77G>C	XP_016856761.1:p.Cys26Ser
NM_000228.3:c.77G>C MANE Select	NP_000219.2:p.Cys26Ser
NM_001017402.2:c.77G>C	NP_001017402.1:p.Cys26Ser