Canonical Allele Identifier: CA2512184949

Gene: LIN28B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104956353T>C , CM000668.2:g.104956353T>C	GRCh38
NC_000006.11:g.105404228T>C , CM000668.1:g.105404228T>C	GRCh37
NC_000006.10:g.105510921T>C	NCBI36
NG_032815.1:g.4306T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000635857.1:c.68-1746T>C	ENSP00000489735.1:n.68-1746T>C
ENST00000637759.1:c.35-1746T>C	ENSP00000490468.1:n.35-1746T>C
XM_006715477.2:c.68-1746T>C	XP_006715540.2:n.68-1746T>C
XM_011535818.1:c.35-1746T>C	XP_011534120.1:n.35-1746T>C
XM_011535818.3:c.35-1746T>C	XP_011534120.1:n.35-1746T>C