Canonical Allele Identifier: CA423027975
Gene: LAMB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.209788625G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209615280G>A , CM000663.2:g.209615280G>A GRCh38
NC_000001.10:g.209788625G>A , CM000663.1:g.209788625G>A GRCh37
NC_000001.9:g.207855248G>A NCBI36
NG_007116.1:g.42196C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.3510C>T MANE Select ENSP00000348384.3:p.Thr1170=
ENST00000356082.8:c.3510C>T ENSP00000348384.3:p.Thr1170=
ENST00000367030.7:c.3510C>T ENSP00000355997.3:p.Thr1170=
ENST00000391911.5:c.3510C>T ENSP00000375778.1:p.Thr1170=
NM_000228.2:c.3510C>T NP_000219.2:p.Thr1170=
NM_001017402.1:c.3510C>T NP_001017402.1:p.Thr1170=
NM_001127641.1:c.3510C>T NP_001121113.1:p.Thr1170=
XM_005273124.3:c.3510C>T XP_005273181.1:p.Thr1170=
XM_005273124.4:c.3510C>T XP_005273181.1:p.Thr1170=
XM_017001272.2:c.3318C>T XP_016856761.1:p.Thr1106=
NM_000228.3:c.3510C>T MANE Select NP_000219.2:p.Thr1170=
NM_001017402.2:c.3510C>T NP_001017402.1:p.Thr1170=