Canonical Allele Identifier: CA1652782533

Gene: LIN28B

Linked Data

• dbSNP Id: rs1769695974

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104959945_104959946del , CM000668.2:g.104959945_104959946del	GRCh38
NC_000006.11:g.105407820_105407821del , CM000668.1:g.105407820_105407821del	GRCh37
NC_000006.10:g.105514513_105514514del	NCBI36
NG_032815.1:g.7898_7899del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.198+1659_198+1660del MANE Select	ENSP00000344401.4:n.198+1659_198+1660del
ENST00000635857.1:c.255+1659_255+1660del	ENSP00000489735.1:n.255+1659_255+1660del
ENST00000637759.1:c.222+1659_222+1660del	ENSP00000490468.1:n.222+1659_222+1660del
ENST00000345080.4:c.198+1659_198+1660del	ENSP00000344401.4:n.198+1659_198+1660del
NM_001004317.3:c.198+1659_198+1660del	NP_001004317.1:n.198+1659_198+1660del
XM_006715477.2:c.255+1659_255+1660del	XP_006715540.2:n.255+1659_255+1660del
XM_011535818.1:c.222+1659_222+1660del	XP_011534120.1:n.222+1659_222+1660del
XM_011535818.3:c.222+1659_222+1660del	XP_011534120.1:n.222+1659_222+1660del
NM_001004317.4:c.198+1659_198+1660del MANE Select	NP_001004317.1:n.198+1659_198+1660del