Canonical Allele Identifier: CA569438787
Gene: LIN28B HGNC NCBI

Linked Data

dbSNP Id: rs1445293306
gnomAD v2: 6-105404248-GC-G
gnomAD v3: 6-104956373-GC-G
gnomAD v4: 6-104956373-GC-G
MyVariant Identifiers: chr6:g.105404249del (hg19) chr6:g.104956374del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104956374del , CM000668.2:g.104956374del GRCh38
NC_000006.11:g.105404249del , CM000668.1:g.105404249del GRCh37
NC_000006.10:g.105510942del NCBI36
NG_032815.1:g.4327del

Transcript Alleles

HGVS Amino-acid change
ENST00000635857.1:c.68-1725del ENSP00000489735.1:n.68-1725del
ENST00000637759.1:c.35-1725del ENSP00000490468.1:n.35-1725del
XM_006715477.2:c.68-1725del XP_006715540.2:n.68-1725del
XM_011535818.1:c.35-1725del XP_011534120.1:n.35-1725del
XM_011535818.3:c.35-1725del XP_011534120.1:n.35-1725del
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