Canonical Allele Identifier: CA1652779458

Gene: LIN28B

Linked Data

• dbSNP Id: rs1778291670

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104956431G>A , CM000668.2:g.104956431G>A	GRCh38
NC_000006.11:g.105404306G>A , CM000668.1:g.105404306G>A	GRCh37
NC_000006.10:g.105510999G>A	NCBI36
NG_032815.1:g.4384G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635857.1:c.68-1668G>A	ENSP00000489735.1:n.68-1668G>A
ENST00000637759.1:c.35-1668G>A	ENSP00000490468.1:n.35-1668G>A
XM_006715477.2:c.68-1668G>A	XP_006715540.2:n.68-1668G>A
XM_011535818.1:c.35-1668G>A	XP_011534120.1:n.35-1668G>A
XM_011535818.3:c.35-1668G>A	XP_011534120.1:n.35-1668G>A