Canonical Allele Identifier: CA816663108

Gene: LIN28B

Linked Data

• dbSNP Id: rs1417737524
• gnomAD v3: 6-104996222-G-A
• gnomAD v4: 6-104996222-G-A
• MyVariant Identifiers: chr6:g.105444097G>A (hg19) ; chr6:g.104996222G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104996222G>A , CM000668.2:g.104996222G>A	GRCh38
NC_000006.11:g.105444097G>A , CM000668.1:g.105444097G>A	GRCh37
NC_000006.10:g.105550790G>A	NCBI36
NG_032815.1:g.44175G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.199-30076G>A MANE Select	ENSP00000344401.4:n.199-30076G>A
ENST00000635857.1:c.256-30076G>A	ENSP00000489735.1:n.256-30076G>A
ENST00000637759.1:c.223-30076G>A	ENSP00000490468.1:n.223-30076G>A
ENST00000345080.4:c.199-30076G>A	ENSP00000344401.4:n.199-30076G>A
NM_001004317.3:c.199-30076G>A	NP_001004317.1:n.199-30076G>A
XM_006715477.2:c.256-30076G>A	XP_006715540.2:n.256-30076G>A
XM_011535818.1:c.223-30076G>A	XP_011534120.1:n.223-30076G>A
XM_011535818.3:c.223-30076G>A	XP_011534120.1:n.223-30076G>A
NM_001004317.4:c.199-30076G>A MANE Select	NP_001004317.1:n.199-30076G>A