Canonical Allele Identifier: CA816663090

Gene: LIN28B

Linked Data

• dbSNP Id: rs1361002794
• gnomAD v3: 6-104996117-C-T
• gnomAD v4: 6-104996117-C-T
• MyVariant Identifiers: chr6:g.105443992C>T (hg19) ; chr6:g.104996117C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104996117C>T , CM000668.2:g.104996117C>T	GRCh38
NC_000006.11:g.105443992C>T , CM000668.1:g.105443992C>T	GRCh37
NC_000006.10:g.105550685C>T	NCBI36
NG_032815.1:g.44070C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.199-30181C>T MANE Select	ENSP00000344401.4:n.199-30181C>T
ENST00000635857.1:c.256-30181C>T	ENSP00000489735.1:n.256-30181C>T
ENST00000637759.1:c.223-30181C>T	ENSP00000490468.1:n.223-30181C>T
ENST00000345080.4:c.199-30181C>T	ENSP00000344401.4:n.199-30181C>T
NM_001004317.3:c.199-30181C>T	NP_001004317.1:n.199-30181C>T
XM_006715477.2:c.256-30181C>T	XP_006715540.2:n.256-30181C>T
XM_011535818.1:c.223-30181C>T	XP_011534120.1:n.223-30181C>T
XM_011535818.3:c.223-30181C>T	XP_011534120.1:n.223-30181C>T
NM_001004317.4:c.199-30181C>T MANE Select	NP_001004317.1:n.199-30181C>T