Canonical Allele Identifier: CA816663017

Gene: LIN28B

Linked Data

• dbSNP Id: rs1299279371
• gnomAD v3: 6-104995845-A-AG
• gnomAD v4: 6-104995845-A-AG
• MyVariant Identifiers: chr6:g.105443720_105443721insG (hg19) ; chr6:g.104995845_104995846insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104995845_104995846insG , CM000668.2:g.104995845_104995846insG	GRCh38
NC_000006.11:g.105443720_105443721insG , CM000668.1:g.105443720_105443721insG	GRCh37
NC_000006.10:g.105550413_105550414insG	NCBI36
NG_032815.1:g.43798_43799insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.199-30453_199-30452insG MANE Select	ENSP00000344401.4:n.199-30453_199-30452insG
ENST00000635857.1:c.256-30453_256-30452insG	ENSP00000489735.1:n.256-30453_256-30452insG
ENST00000637759.1:c.223-30453_223-30452insG	ENSP00000490468.1:n.223-30453_223-30452insG
ENST00000345080.4:c.199-30453_199-30452insG	ENSP00000344401.4:n.199-30453_199-30452insG
NM_001004317.3:c.199-30453_199-30452insG	NP_001004317.1:n.199-30453_199-30452insG
XM_006715477.2:c.256-30453_256-30452insG	XP_006715540.2:n.256-30453_256-30452insG
XM_011535818.1:c.223-30453_223-30452insG	XP_011534120.1:n.223-30453_223-30452insG
XM_011535818.3:c.223-30453_223-30452insG	XP_011534120.1:n.223-30453_223-30452insG
NM_001004317.4:c.199-30453_199-30452insG MANE Select	NP_001004317.1:n.199-30453_199-30452insG