Canonical Allele Identifier: CA1652779366
Gene: LIN28B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104956328T= , CM000668.2:g.104956328T= GRCh38
NC_000006.11:g.105404203T= , CM000668.1:g.105404203T= GRCh37
NC_000006.10:g.105510896T= NCBI36
NG_032815.1:g.4281T=

Transcript Alleles

HGVS Amino-acid change
ENST00000635857.1:c.68-1771T= ENSP00000489735.1:n.68-1771T=
ENST00000637759.1:c.35-1771T= ENSP00000490468.1:n.35-1771T=
XM_006715477.2:c.68-1771T= XP_006715540.2:n.68-1771T=
XM_011535818.1:c.35-1771T= XP_011534120.1:n.35-1771T=
XM_011535818.3:c.35-1771T= XP_011534120.1:n.35-1771T=
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