Canonical Allele Identifier: CA145434056

Gene: LIN28B

Linked Data

• dbSNP Id: rs898948197
• gnomAD v2: 6-105407846-GAAC-G
• gnomAD v3: 6-104959971-GAAC-G
• gnomAD v4: 6-104959971-GAAC-G
• MyVariant Identifiers: chr6:g.105407847_105407849del (hg19) ; chr6:g.104959972_104959974del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104959977_104959979del , CM000668.2:g.104959977_104959979del	GRCh38
NC_000006.11:g.105407852_105407854del , CM000668.1:g.105407852_105407854del	GRCh37
NC_000006.10:g.105514545_105514547del	NCBI36
NG_032815.1:g.7930_7932del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.198+1691_198+1693del MANE Select	ENSP00000344401.4:n.198+1691_198+1693del
ENST00000635857.1:c.255+1691_255+1693del	ENSP00000489735.1:n.255+1691_255+1693del
ENST00000637759.1:c.222+1691_222+1693del	ENSP00000490468.1:n.222+1691_222+1693del
ENST00000345080.4:c.198+1691_198+1693del	ENSP00000344401.4:n.198+1691_198+1693del
NM_001004317.3:c.198+1691_198+1693del	NP_001004317.1:n.198+1691_198+1693del
XM_006715477.2:c.255+1691_255+1693del	XP_006715540.2:n.255+1691_255+1693del
XM_011535818.1:c.222+1691_222+1693del	XP_011534120.1:n.222+1691_222+1693del
XM_011535818.3:c.222+1691_222+1693del	XP_011534120.1:n.222+1691_222+1693del
NM_001004317.4:c.198+1691_198+1693del MANE Select	NP_001004317.1:n.198+1691_198+1693del