Canonical Allele Identifier: CA1652782449

Gene: LIN28B

Linked Data

• dbSNP Id: rs1769693958

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104959854T>C , CM000668.2:g.104959854T>C	GRCh38
NC_000006.11:g.105407729T>C , CM000668.1:g.105407729T>C	GRCh37
NC_000006.10:g.105514422T>C	NCBI36
NG_032815.1:g.7807T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.198+1568T>C MANE Select	ENSP00000344401.4:n.198+1568T>C
ENST00000635857.1:c.255+1568T>C	ENSP00000489735.1:n.255+1568T>C
ENST00000637759.1:c.222+1568T>C	ENSP00000490468.1:n.222+1568T>C
ENST00000345080.4:c.198+1568T>C	ENSP00000344401.4:n.198+1568T>C
NM_001004317.3:c.198+1568T>C	NP_001004317.1:n.198+1568T>C
XM_006715477.2:c.255+1568T>C	XP_006715540.2:n.255+1568T>C
XM_011535818.1:c.222+1568T>C	XP_011534120.1:n.222+1568T>C
XM_011535818.3:c.222+1568T>C	XP_011534120.1:n.222+1568T>C
NM_001004317.4:c.198+1568T>C MANE Select	NP_001004317.1:n.198+1568T>C