Canonical Allele Identifier: CA1652782419
Gene: LIN28B HGNC NCBI

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=