Canonical Allele Identifier: CA433835560
Gene: LAMB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.49168569G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49131136G>A , CM000665.2:g.49131136G>A GRCh38
NC_000003.11:g.49168569G>A , CM000665.1:g.49168569G>A GRCh37
NC_000003.10:g.49143573G>A NCBI36
NG_008094.1:g.7031C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.729C>T MANE Select ENSP00000307156.4:p.Thr243=
ENST00000305544.8:c.729C>T ENSP00000307156.4:p.Thr243=
ENST00000418109.5:c.729C>T ENSP00000388325.1:p.Thr243=
ENST00000494831.1:c.282C>T ENSP00000444751.1:p.Thr94=
NM_002292.3:c.729C>T NP_002283.3:p.Thr243=
XM_005265127.3:c.729C>T XP_005265184.1:p.Thr243=
XM_005265127.4:c.729C>T XP_005265184.1:p.Thr243=
NM_002292.4:c.729C>T MANE Select NP_002283.3:p.Thr243=