Canonical Allele Identifier: CA1652782419

Gene: LIN28B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104959808T= , CM000668.2:g.104959808T=	GRCh38
NC_000006.11:g.105407683T= , CM000668.1:g.105407683T=	GRCh37
NC_000006.10:g.105514376T=	NCBI36
NG_032815.1:g.7761T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.198+1522T= MANE Select	ENSP00000344401.4:n.198+1522T=
ENST00000635857.1:c.255+1522T=	ENSP00000489735.1:n.255+1522T=
ENST00000637759.1:c.222+1522T=	ENSP00000490468.1:n.222+1522T=
ENST00000345080.4:c.198+1522T=	ENSP00000344401.4:n.198+1522T=
NM_001004317.3:c.198+1522T=	NP_001004317.1:n.198+1522T=
XM_006715477.2:c.255+1522T=	XP_006715540.2:n.255+1522T=
XM_011535818.1:c.222+1522T=	XP_011534120.1:n.222+1522T=
XM_011535818.3:c.222+1522T=	XP_011534120.1:n.222+1522T=
NM_001004317.4:c.198+1522T= MANE Select	NP_001004317.1:n.198+1522T=