Canonical Allele Identifier: CA816646685

Gene: LIN28B

Linked Data

• dbSNP Id: rs314277
• gnomAD v3: 6-104959787-A-G
• gnomAD v4: 6-104959787-A-G
• MyVariant Identifiers: chr6:g.105407662A>G (hg19) ; chr6:g.104959787A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104959787A>G , CM000668.2:g.104959787A>G	GRCh38
NC_000006.11:g.105407662A>G , CM000668.1:g.105407662A>G	GRCh37
NC_000006.10:g.105514355A>G	NCBI36
NG_032815.1:g.7740A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000345080.5:c.198+1501A>G MANE Select	ENSP00000344401.4:n.198+1501A>G
ENST00000635857.1:c.255+1501A>G	ENSP00000489735.1:n.255+1501A>G
ENST00000637759.1:c.222+1501A>G	ENSP00000490468.1:n.222+1501A>G
ENST00000345080.4:c.198+1501A>G	ENSP00000344401.4:n.198+1501A>G
NM_001004317.3:c.198+1501A>G	NP_001004317.1:n.198+1501A>G
XM_006715477.2:c.255+1501A>G	XP_006715540.2:n.255+1501A>G
XM_011535818.1:c.222+1501A>G	XP_011534120.1:n.222+1501A>G
XM_011535818.3:c.222+1501A>G	XP_011534120.1:n.222+1501A>G
NM_001004317.4:c.198+1501A>G MANE Select	NP_001004317.1:n.198+1501A>G