Canonical Allele Identifier: CA1652782370

Gene: LIN28B

Linked Data

• dbSNP Id: rs1769686401

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104959678_104959689del , CM000668.2:g.104959678_104959689del	GRCh38
NC_000006.11:g.105407553_105407564del , CM000668.1:g.105407553_105407564del	GRCh37
NC_000006.10:g.105514246_105514257del	NCBI36
NG_032815.1:g.7631_7642del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.198+1392_198+1403del MANE Select	ENSP00000344401.4:n.198+1392_198+1403del
ENST00000635857.1:c.255+1392_255+1403del	ENSP00000489735.1:n.255+1392_255+1403del
ENST00000637759.1:c.222+1392_222+1403del	ENSP00000490468.1:n.222+1392_222+1403del
ENST00000345080.4:c.198+1392_198+1403del	ENSP00000344401.4:n.198+1392_198+1403del
NM_001004317.3:c.198+1392_198+1403del	NP_001004317.1:n.198+1392_198+1403del
XM_006715477.2:c.255+1392_255+1403del	XP_006715540.2:n.255+1392_255+1403del
XM_011535818.1:c.222+1392_222+1403del	XP_011534120.1:n.222+1392_222+1403del
XM_011535818.3:c.222+1392_222+1403del	XP_011534120.1:n.222+1392_222+1403del
NM_001004317.4:c.198+1392_198+1403del MANE Select	NP_001004317.1:n.198+1392_198+1403del