Canonical Allele Identifier: CA1652781072
Gene: LIN28B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104958308C= , CM000668.2:g.104958308C= GRCh38
NC_000006.11:g.105406183C= , CM000668.1:g.105406183C= GRCh37
NC_000006.10:g.105512876C= NCBI36
NG_032815.1:g.6261C=

Transcript Alleles

HGVS Amino-acid change
ENST00000345080.5:c.198+22C= MANE Select ENSP00000344401.4:n.198+22C=
ENST00000635857.1:c.255+22C= ENSP00000489735.1:n.255+22C=
ENST00000637759.1:c.222+22C= ENSP00000490468.1:n.222+22C=
ENST00000345080.4:c.198+22C= ENSP00000344401.4:n.198+22C=
NM_001004317.3:c.198+22C= NP_001004317.1:n.198+22C=
XM_006715477.2:c.255+22C= XP_006715540.2:n.255+22C=
XM_011535818.1:c.222+22C= XP_011534120.1:n.222+22C=
XM_011535818.3:c.222+22C= XP_011534120.1:n.222+22C=
NM_001004317.4:c.198+22C= MANE Select NP_001004317.1:n.198+22C=
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