Canonical Allele Identifier: CA816644165

Gene: LIN28B

Linked Data

• dbSNP Id: rs1452821897
• gnomAD v3: 6-104956330-T-C
• gnomAD v4: 6-104956330-T-C
• MyVariant Identifiers: chr6:g.105404205T>C (hg19) ; chr6:g.104956330T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104956330T>C , CM000668.2:g.104956330T>C	GRCh38
NC_000006.11:g.105404205T>C , CM000668.1:g.105404205T>C	GRCh37
NC_000006.10:g.105510898T>C	NCBI36
NG_032815.1:g.4283T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000635857.1:c.68-1769T>C	ENSP00000489735.1:n.68-1769T>C
ENST00000637759.1:c.35-1769T>C	ENSP00000490468.1:n.35-1769T>C
XM_006715477.2:c.68-1769T>C	XP_006715540.2:n.68-1769T>C
XM_011535818.1:c.35-1769T>C	XP_011534120.1:n.35-1769T>C
XM_011535818.3:c.35-1769T>C	XP_011534120.1:n.35-1769T>C