Canonical Allele Identifier: CA1652771553

Gene: LIN28B

Linked Data

• dbSNP Id: rs1582885844

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104996223T>G , CM000668.2:g.104996223T>G	GRCh38
NC_000006.11:g.105444098T>G , CM000668.1:g.105444098T>G	GRCh37
NC_000006.10:g.105550791T>G	NCBI36
NG_032815.1:g.44176T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.199-30075T>G MANE Select	ENSP00000344401.4:n.199-30075T>G
ENST00000635857.1:c.256-30075T>G	ENSP00000489735.1:n.256-30075T>G
ENST00000637759.1:c.223-30075T>G	ENSP00000490468.1:n.223-30075T>G
ENST00000345080.4:c.199-30075T>G	ENSP00000344401.4:n.199-30075T>G
NM_001004317.3:c.199-30075T>G	NP_001004317.1:n.199-30075T>G
XM_006715477.2:c.256-30075T>G	XP_006715540.2:n.256-30075T>G
XM_011535818.1:c.223-30075T>G	XP_011534120.1:n.223-30075T>G
XM_011535818.3:c.223-30075T>G	XP_011534120.1:n.223-30075T>G
NM_001004317.4:c.199-30075T>G MANE Select	NP_001004317.1:n.199-30075T>G