Canonical Allele Identifier: CA145434035
Gene: LIN28B HGNC NCBI

Linked Data

dbSNP Id: rs952760600

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104959832A>G , CM000668.2:g.104959832A>G GRCh38
NC_000006.11:g.105407707A>G , CM000668.1:g.105407707A>G GRCh37
NC_000006.10:g.105514400A>G NCBI36
NG_032815.1:g.7785A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000345080.5:c.198+1546A>G MANE Select ENSP00000344401.4:n.198+1546A>G
ENST00000635857.1:c.255+1546A>G ENSP00000489735.1:n.255+1546A>G
ENST00000637759.1:c.222+1546A>G ENSP00000490468.1:n.222+1546A>G
ENST00000345080.4:c.198+1546A>G ENSP00000344401.4:n.198+1546A>G
NM_001004317.3:c.198+1546A>G NP_001004317.1:n.198+1546A>G
XM_006715477.2:c.255+1546A>G XP_006715540.2:n.255+1546A>G
XM_011535818.1:c.222+1546A>G XP_011534120.1:n.222+1546A>G
XM_011535818.3:c.222+1546A>G XP_011534120.1:n.222+1546A>G
NM_001004317.4:c.198+1546A>G MANE Select NP_001004317.1:n.198+1546A>G