Canonical Allele Identifier: CA816644169

Gene: LIN28B

Linked Data

• dbSNP Id: rs1208848693
• gnomAD v3: 6-104956340-C-T
• gnomAD v4: 6-104956340-C-T
• MyVariant Identifiers: chr6:g.105404215C>T (hg19) ; chr6:g.104956340C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104956340C>T , CM000668.2:g.104956340C>T	GRCh38
NC_000006.11:g.105404215C>T , CM000668.1:g.105404215C>T	GRCh37
NC_000006.10:g.105510908C>T	NCBI36
NG_032815.1:g.4293C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000635857.1:c.68-1759C>T	ENSP00000489735.1:n.68-1759C>T
ENST00000637759.1:c.35-1759C>T	ENSP00000490468.1:n.35-1759C>T
XM_006715477.2:c.68-1759C>T	XP_006715540.2:n.68-1759C>T
XM_011535818.1:c.35-1759C>T	XP_011534120.1:n.35-1759C>T
XM_011535818.3:c.35-1759C>T	XP_011534120.1:n.35-1759C>T