Canonical Allele Identifier: CA2525235019
Gene: LAMB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49131138_49131139insCATTAAAA , CM000665.2:g.49131138_49131139insCATTAAAA GRCh38
NC_000003.11:g.49168571_49168572insCATTAAAA , CM000665.1:g.49168571_49168572insCATTAAAA GRCh37
NC_000003.10:g.49143575_49143576insCATTAAAA NCBI36
NG_008094.1:g.7028_7029insTTTTAATG

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.726_727insTTTTAATG MANE Select ENSP00000307156.4:p.Thr243PhefsTer2
ENST00000305544.8:c.726_727insTTTTAATG ENSP00000307156.4:p.Thr243PhefsTer2
ENST00000418109.5:c.726_727insTTTTAATG ENSP00000388325.1:p.Thr243PhefsTer2
ENST00000494831.1:c.279_280insTTTTAATG ENSP00000444751.1:p.Thr94PhefsTer2
NM_002292.3:c.726_727insTTTTAATG NP_002283.3:p.Thr243PhefsTer2
XM_005265127.3:c.726_727insTTTTAATG XP_005265184.1:p.Thr243PhefsTer2
XM_005265127.4:c.726_727insTTTTAATG XP_005265184.1:p.Thr243PhefsTer2
NM_002292.4:c.726_727insTTTTAATG MANE Select NP_002283.3:p.Thr243PhefsTer2