Canonical Allele Identifier: CA145433657

Gene: LIN28B

Linked Data

• dbSNP Id: rs150072422
• gnomAD v3: 6-104956368-A-G
• MyVariant Identifiers: chr6:g.105404243A>G (hg19) ; chr6:g.104956368A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104956368A>G , CM000668.2:g.104956368A>G	GRCh38
NC_000006.11:g.105404243A>G , CM000668.1:g.105404243A>G	GRCh37
NC_000006.10:g.105510936A>G	NCBI36
NG_032815.1:g.4321A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000635857.1:c.68-1731A>G	ENSP00000489735.1:n.68-1731A>G
ENST00000637759.1:c.35-1731A>G	ENSP00000490468.1:n.35-1731A>G
XM_006715477.2:c.68-1731A>G	XP_006715540.2:n.68-1731A>G
XM_011535818.1:c.35-1731A>G	XP_011534120.1:n.35-1731A>G
XM_011535818.3:c.35-1731A>G	XP_011534120.1:n.35-1731A>G