Canonical Allele Identifier: CA569565605

Gene: LIN28B

Linked Data

• dbSNP Id: rs1562071338
• gnomAD v2: 6-105406185-CTCT-C
• gnomAD v4: 6-104958310-CTCT-C
• MyVariant Identifiers: chr6:g.105406186_105406188del (hg19) ; chr6:g.104958311_104958313del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104958313_104958315del , CM000668.2:g.104958313_104958315del	GRCh38
NC_000006.11:g.105406188_105406190del , CM000668.1:g.105406188_105406190del	GRCh37
NC_000006.10:g.105512881_105512883del	NCBI36
NG_032815.1:g.6266_6268del

Transcript Alleles

HGVS	Amino-acid change
ENST00000345080.5:c.198+27_198+29del MANE Select	ENSP00000344401.4:n.198+27_198+29del
ENST00000635857.1:c.255+27_255+29del	ENSP00000489735.1:n.255+27_255+29del
ENST00000637759.1:c.222+27_222+29del	ENSP00000490468.1:n.222+27_222+29del
ENST00000345080.4:c.198+27_198+29del	ENSP00000344401.4:n.198+27_198+29del
NM_001004317.3:c.198+27_198+29del	NP_001004317.1:n.198+27_198+29del
XM_006715477.2:c.255+27_255+29del	XP_006715540.2:n.255+27_255+29del
XM_011535818.1:c.222+27_222+29del	XP_011534120.1:n.222+27_222+29del
XM_011535818.3:c.222+27_222+29del	XP_011534120.1:n.222+27_222+29del
NM_001004317.4:c.198+27_198+29del MANE Select	NP_001004317.1:n.198+27_198+29del