Canonical Allele Identifier: CA1652779456

Gene: LIN28B

Linked Data

• dbSNP Id: rs1778291704
• gnomAD v3: 6-104956430-GGTTTACCTAA-G
• gnomAD v4: 6-104956430-GGTTTACCTAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104956431_104956440del , CM000668.2:g.104956431_104956440del	GRCh38
NC_000006.11:g.105404306_105404315del , CM000668.1:g.105404306_105404315del	GRCh37
NC_000006.10:g.105510999_105511008del	NCBI36
NG_032815.1:g.4384_4393del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635857.1:c.68-1668_68-1659del	ENSP00000489735.1:n.68-1668_68-1659del
ENST00000637759.1:c.35-1668_35-1659del	ENSP00000490468.1:n.35-1668_35-1659del
XM_006715477.2:c.68-1668_68-1659del	XP_006715540.2:n.68-1668_68-1659del
XM_011535818.1:c.35-1668_35-1659del	XP_011534120.1:n.35-1668_35-1659del
XM_011535818.3:c.35-1668_35-1659del	XP_011534120.1:n.35-1668_35-1659del