Canonical Allele Identifier: CA145433667

Gene: LIN28B

Linked Data

• dbSNP Id: rs926044835
• gnomAD v3: 6-104956443-A-C
• gnomAD v4: 6-104956443-A-C
• MyVariant Identifiers: chr6:g.105404318A>C (hg19) ; chr6:g.104956443A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104956443A>C , CM000668.2:g.104956443A>C	GRCh38
NC_000006.11:g.105404318A>C , CM000668.1:g.105404318A>C	GRCh37
NC_000006.10:g.105511011A>C	NCBI36
NG_032815.1:g.4396A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635857.1:c.68-1656A>C	ENSP00000489735.1:n.68-1656A>C
ENST00000637759.1:c.35-1656A>C	ENSP00000490468.1:n.35-1656A>C
XM_006715477.2:c.68-1656A>C	XP_006715540.2:n.68-1656A>C
XM_011535818.1:c.35-1656A>C	XP_011534120.1:n.35-1656A>C
XM_011535818.3:c.35-1656A>C	XP_011534120.1:n.35-1656A>C