Canonical Allele Identifier: CA1652771412

Gene: LIN28B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104995898_104995899delinsCT , CM000668.2:g.104995898_104995899delinsCT	GRCh38
NC_000006.11:g.105443773_105443774delinsCT , CM000668.1:g.105443773_105443774delinsCT	GRCh37
NC_000006.10:g.105550466_105550467delinsCT	NCBI36
NG_032815.1:g.43851_43852delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.199-30400_199-30399delinsCT MANE Select	ENSP00000344401.4:n.199-30400_199-30399delinsCT
ENST00000635857.1:c.256-30400_256-30399delinsCT	ENSP00000489735.1:n.256-30400_256-30399delinsCT
ENST00000637759.1:c.223-30400_223-30399delinsCT	ENSP00000490468.1:n.223-30400_223-30399delinsCT
ENST00000345080.4:c.199-30400_199-30399delinsCT	ENSP00000344401.4:n.199-30400_199-30399delinsCT
NM_001004317.3:c.199-30400_199-30399delinsCT	NP_001004317.1:n.199-30400_199-30399delinsCT
XM_006715477.2:c.256-30400_256-30399delinsCT	XP_006715540.2:n.256-30400_256-30399delinsCT
XM_011535818.1:c.223-30400_223-30399delinsCT	XP_011534120.1:n.223-30400_223-30399delinsCT
XM_011535818.3:c.223-30400_223-30399delinsCT	XP_011534120.1:n.223-30400_223-30399delinsCT
NM_001004317.4:c.199-30400_199-30399delinsCT MANE Select	NP_001004317.1:n.199-30400_199-30399delinsCT