Canonical Allele Identifier: CA569439366

Gene: LIN28B

Linked Data

• dbSNP Id: rs1307854022
• gnomAD v2: 6-105407680-GGTT-G
• gnomAD v3: 6-104959805-GGTT-G
• gnomAD v4: 6-104959805-GGTT-G
• MyVariant Identifiers: chr6:g.105407681_105407683del (hg19) ; chr6:g.104959806_104959808del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104959809_104959811del , CM000668.2:g.104959809_104959811del	GRCh38
NC_000006.11:g.105407684_105407686del , CM000668.1:g.105407684_105407686del	GRCh37
NC_000006.10:g.105514377_105514379del	NCBI36
NG_032815.1:g.7762_7764del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.198+1523_198+1525del MANE Select	ENSP00000344401.4:n.198+1523_198+1525del
ENST00000635857.1:c.255+1523_255+1525del	ENSP00000489735.1:n.255+1523_255+1525del
ENST00000637759.1:c.222+1523_222+1525del	ENSP00000490468.1:n.222+1523_222+1525del
ENST00000345080.4:c.198+1523_198+1525del	ENSP00000344401.4:n.198+1523_198+1525del
NM_001004317.3:c.198+1523_198+1525del	NP_001004317.1:n.198+1523_198+1525del
XM_006715477.2:c.255+1523_255+1525del	XP_006715540.2:n.255+1523_255+1525del
XM_011535818.1:c.222+1523_222+1525del	XP_011534120.1:n.222+1523_222+1525del
XM_011535818.3:c.222+1523_222+1525del	XP_011534120.1:n.222+1523_222+1525del
NM_001004317.4:c.198+1523_198+1525del MANE Select	NP_001004317.1:n.198+1523_198+1525del