Canonical Allele Identifier: CA1652771387

Gene: LIN28B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104995845_104995846delinsAT , CM000668.2:g.104995845_104995846delinsAT	GRCh38
NC_000006.11:g.105443720_105443721delinsAT , CM000668.1:g.105443720_105443721delinsAT	GRCh37
NC_000006.10:g.105550413_105550414delinsAT	NCBI36
NG_032815.1:g.43798_43799delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.199-30453_199-30452delinsAT MANE Select	ENSP00000344401.4:n.199-30453_199-30452delinsAT
ENST00000635857.1:c.256-30453_256-30452delinsAT	ENSP00000489735.1:n.256-30453_256-30452delinsAT
ENST00000637759.1:c.223-30453_223-30452delinsAT	ENSP00000490468.1:n.223-30453_223-30452delinsAT
ENST00000345080.4:c.199-30453_199-30452delinsAT	ENSP00000344401.4:n.199-30453_199-30452delinsAT
NM_001004317.3:c.199-30453_199-30452delinsAT	NP_001004317.1:n.199-30453_199-30452delinsAT
XM_006715477.2:c.256-30453_256-30452delinsAT	XP_006715540.2:n.256-30453_256-30452delinsAT
XM_011535818.1:c.223-30453_223-30452delinsAT	XP_011534120.1:n.223-30453_223-30452delinsAT
XM_011535818.3:c.223-30453_223-30452delinsAT	XP_011534120.1:n.223-30453_223-30452delinsAT
NM_001004317.4:c.199-30453_199-30452delinsAT MANE Select	NP_001004317.1:n.199-30453_199-30452delinsAT