Canonical Allele Identifier: CA145434022

Gene: LIN28B

Linked Data

• dbSNP Id: rs574974995
• gnomAD v3: 6-104959711-T-A
• gnomAD v4: 6-104959711-T-A
• MyVariant Identifiers: chr6:g.105407586T>A (hg19) ; chr6:g.104959711T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104959711T>A , CM000668.2:g.104959711T>A	GRCh38
NC_000006.11:g.105407586T>A , CM000668.1:g.105407586T>A	GRCh37
NC_000006.10:g.105514279T>A	NCBI36
NG_032815.1:g.7664T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.198+1425T>A MANE Select	ENSP00000344401.4:n.198+1425T>A
ENST00000635857.1:c.255+1425T>A	ENSP00000489735.1:n.255+1425T>A
ENST00000637759.1:c.222+1425T>A	ENSP00000490468.1:n.222+1425T>A
ENST00000345080.4:c.198+1425T>A	ENSP00000344401.4:n.198+1425T>A
NM_001004317.3:c.198+1425T>A	NP_001004317.1:n.198+1425T>A
XM_006715477.2:c.255+1425T>A	XP_006715540.2:n.255+1425T>A
XM_011535818.1:c.222+1425T>A	XP_011534120.1:n.222+1425T>A
XM_011535818.3:c.222+1425T>A	XP_011534120.1:n.222+1425T>A
NM_001004317.4:c.198+1425T>A MANE Select	NP_001004317.1:n.198+1425T>A