Canonical Allele Identifier: CA1652782543
Gene: LIN28B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104959958A= , CM000668.2:g.104959958A= GRCh38
NC_000006.11:g.105407833A= , CM000668.1:g.105407833A= GRCh37
NC_000006.10:g.105514526A= NCBI36
NG_032815.1:g.7911A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000345080.5:c.198+1672A= MANE Select ENSP00000344401.4:n.198+1672A=
ENST00000635857.1:c.255+1672A= ENSP00000489735.1:n.255+1672A=
ENST00000637759.1:c.222+1672A= ENSP00000490468.1:n.222+1672A=
ENST00000345080.4:c.198+1672A= ENSP00000344401.4:n.198+1672A=
NM_001004317.3:c.198+1672A= NP_001004317.1:n.198+1672A=
XM_006715477.2:c.255+1672A= XP_006715540.2:n.255+1672A=
XM_011535818.1:c.222+1672A= XP_011534120.1:n.222+1672A=
XM_011535818.3:c.222+1672A= XP_011534120.1:n.222+1672A=
NM_001004317.4:c.198+1672A= MANE Select NP_001004317.1:n.198+1672A=