Canonical Allele Identifier: CA569443486

Gene: LIN28B

Linked Data

• dbSNP Id: rs201567101
• gnomAD v2: 6-105443840-TTATA-T
• gnomAD v3: 6-104995965-TTATA-T
• gnomAD v4: 6-104995965-TTATA-T
• MyVariant Identifiers: chr6:g.105443845_105443848del (hg19) ; chr6:g.104995970_104995973del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104995978_104995981del , CM000668.2:g.104995978_104995981del	GRCh38
NC_000006.11:g.105443853_105443856del , CM000668.1:g.105443853_105443856del	GRCh37
NC_000006.10:g.105550546_105550549del	NCBI36
NG_032815.1:g.43931_43934del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.199-30320_199-30317del MANE Select	ENSP00000344401.4:n.199-30320_199-30317del
ENST00000635857.1:c.256-30320_256-30317del	ENSP00000489735.1:n.256-30320_256-30317del
ENST00000637759.1:c.223-30320_223-30317del	ENSP00000490468.1:n.223-30320_223-30317del
ENST00000345080.4:c.199-30320_199-30317del	ENSP00000344401.4:n.199-30320_199-30317del
NM_001004317.3:c.199-30320_199-30317del	NP_001004317.1:n.199-30320_199-30317del
XM_006715477.2:c.256-30320_256-30317del	XP_006715540.2:n.256-30320_256-30317del
XM_011535818.1:c.223-30320_223-30317del	XP_011534120.1:n.223-30320_223-30317del
XM_011535818.3:c.223-30320_223-30317del	XP_011534120.1:n.223-30320_223-30317del
NM_001004317.4:c.199-30320_199-30317del MANE Select	NP_001004317.1:n.199-30320_199-30317del