Canonical Allele Identifier: CA816646745

Gene: LIN28B

Linked Data

• dbSNP Id: rs1407154181
• MyVariant Identifiers: chr6:g.105407736_105407738del (hg19) ; chr6:g.104959861_104959863del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104959863_104959865del , CM000668.2:g.104959863_104959865del	GRCh38
NC_000006.11:g.105407738_105407740del , CM000668.1:g.105407738_105407740del	GRCh37
NC_000006.10:g.105514431_105514433del	NCBI36
NG_032815.1:g.7816_7818del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.198+1577_198+1579del MANE Select	ENSP00000344401.4:n.198+1577_198+1579del
ENST00000635857.1:c.255+1577_255+1579del	ENSP00000489735.1:n.255+1577_255+1579del
ENST00000637759.1:c.222+1577_222+1579del	ENSP00000490468.1:n.222+1577_222+1579del
ENST00000345080.4:c.198+1577_198+1579del	ENSP00000344401.4:n.198+1577_198+1579del
NM_001004317.3:c.198+1577_198+1579del	NP_001004317.1:n.198+1577_198+1579del
XM_006715477.2:c.255+1577_255+1579del	XP_006715540.2:n.255+1577_255+1579del
XM_011535818.1:c.222+1577_222+1579del	XP_011534120.1:n.222+1577_222+1579del
XM_011535818.3:c.222+1577_222+1579del	XP_011534120.1:n.222+1577_222+1579del
NM_001004317.4:c.198+1577_198+1579del MANE Select	NP_001004317.1:n.198+1577_198+1579del