Canonical Allele Identifier: CA816646645

Gene: LIN28B

Linked Data

• dbSNP Id: rs1227521292
• gnomAD v3: 6-104959717-G-GT
• gnomAD v4: 6-104959717-G-GT
• MyVariant Identifiers: chr6:g.105407592_105407593insT (hg19) ; chr6:g.104959717_104959718insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104959723dup , CM000668.2:g.104959723dup	GRCh38
NC_000006.11:g.105407598dup , CM000668.1:g.105407598dup	GRCh37
NC_000006.10:g.105514291dup	NCBI36
NG_032815.1:g.7676dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.198+1437dup MANE Select	ENSP00000344401.4:n.198+1437dup
ENST00000635857.1:c.255+1437dup	ENSP00000489735.1:n.255+1437dup
ENST00000637759.1:c.222+1437dup	ENSP00000490468.1:n.222+1437dup
ENST00000345080.4:c.198+1437dup	ENSP00000344401.4:n.198+1437dup
NM_001004317.3:c.198+1437dup	NP_001004317.1:n.198+1437dup
XM_006715477.2:c.255+1437dup	XP_006715540.2:n.255+1437dup
XM_011535818.1:c.222+1437dup	XP_011534120.1:n.222+1437dup
XM_011535818.3:c.222+1437dup	XP_011534120.1:n.222+1437dup
NM_001004317.4:c.198+1437dup MANE Select	NP_001004317.1:n.198+1437dup