Canonical Allele Identifier: CA1652771498

Gene: LIN28B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104996074T= , CM000668.2:g.104996074T=	GRCh38
NC_000006.11:g.105443949T= , CM000668.1:g.105443949T=	GRCh37
NC_000006.10:g.105550642T=	NCBI36
NG_032815.1:g.44027T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.199-30224T= MANE Select	ENSP00000344401.4:n.199-30224T=
ENST00000635857.1:c.256-30224T=	ENSP00000489735.1:n.256-30224T=
ENST00000637759.1:c.223-30224T=	ENSP00000490468.1:n.223-30224T=
ENST00000345080.4:c.199-30224T=	ENSP00000344401.4:n.199-30224T=
NM_001004317.3:c.199-30224T=	NP_001004317.1:n.199-30224T=
XM_006715477.2:c.256-30224T=	XP_006715540.2:n.256-30224T=
XM_011535818.1:c.223-30224T=	XP_011534120.1:n.223-30224T=
XM_011535818.3:c.223-30224T=	XP_011534120.1:n.223-30224T=
NM_001004317.4:c.199-30224T= MANE Select	NP_001004317.1:n.199-30224T=