Canonical Allele Identifier: CA145434033
Gene: LIN28B HGNC NCBI

Linked Data

dbSNP Id: rs577329816

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104959817G>T , CM000668.2:g.104959817G>T GRCh38
NC_000006.11:g.105407692G>T , CM000668.1:g.105407692G>T GRCh37
NC_000006.10:g.105514385G>T NCBI36
NG_032815.1:g.7770G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000345080.5:c.198+1531G>T MANE Select ENSP00000344401.4:n.198+1531G>T
ENST00000635857.1:c.255+1531G>T ENSP00000489735.1:n.255+1531G>T
ENST00000637759.1:c.222+1531G>T ENSP00000490468.1:n.222+1531G>T
ENST00000345080.4:c.198+1531G>T ENSP00000344401.4:n.198+1531G>T
NM_001004317.3:c.198+1531G>T NP_001004317.1:n.198+1531G>T
XM_006715477.2:c.255+1531G>T XP_006715540.2:n.255+1531G>T
XM_011535818.1:c.222+1531G>T XP_011534120.1:n.222+1531G>T
XM_011535818.3:c.222+1531G>T XP_011534120.1:n.222+1531G>T
NM_001004317.4:c.198+1531G>T MANE Select NP_001004317.1:n.198+1531G>T