Canonical Allele Identifier: CA145434030

Gene: LIN28B

Linked Data

• dbSNP Id: rs314277
• MyVariant Identifiers: chr6:g.105407662A>T (hg19) ; chr6:g.104959787A>T (hg38)

Genomic Alleles

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

Transcript Alleles

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