Canonical Allele Identifier: CA1652782466

Gene: LIN28B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104959862_104959863delinsAT , CM000668.2:g.104959862_104959863delinsAT	GRCh38
NC_000006.11:g.105407737_105407738delinsAT , CM000668.1:g.105407737_105407738delinsAT	GRCh37
NC_000006.10:g.105514430_105514431delinsAT	NCBI36
NG_032815.1:g.7815_7816delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.198+1576_198+1577delinsAT MANE Select	ENSP00000344401.4:n.198+1576_198+1577delinsAT
ENST00000635857.1:c.255+1576_255+1577delinsAT	ENSP00000489735.1:n.255+1576_255+1577delinsAT
ENST00000637759.1:c.222+1576_222+1577delinsAT	ENSP00000490468.1:n.222+1576_222+1577delinsAT
ENST00000345080.4:c.198+1576_198+1577delinsAT	ENSP00000344401.4:n.198+1576_198+1577delinsAT
NM_001004317.3:c.198+1576_198+1577delinsAT	NP_001004317.1:n.198+1576_198+1577delinsAT
XM_006715477.2:c.255+1576_255+1577delinsAT	XP_006715540.2:n.255+1576_255+1577delinsAT
XM_011535818.1:c.222+1576_222+1577delinsAT	XP_011534120.1:n.222+1576_222+1577delinsAT
XM_011535818.3:c.222+1576_222+1577delinsAT	XP_011534120.1:n.222+1576_222+1577delinsAT
NM_001004317.4:c.198+1576_198+1577delinsAT MANE Select	NP_001004317.1:n.198+1576_198+1577delinsAT