Canonical Allele Identifier: CA1652779388
Gene: LIN28B HGNC NCBI

Linked Data

dbSNP Id: rs1778290581

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104956353T>G , CM000668.2:g.104956353T>G GRCh38
NC_000006.11:g.105404228T>G , CM000668.1:g.105404228T>G GRCh37
NC_000006.10:g.105510921T>G NCBI36
NG_032815.1:g.4306T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000635857.1:c.68-1746T>G ENSP00000489735.1:n.68-1746T>G
ENST00000637759.1:c.35-1746T>G ENSP00000490468.1:n.35-1746T>G
XM_006715477.2:c.68-1746T>G XP_006715540.2:n.68-1746T>G
XM_011535818.1:c.35-1746T>G XP_011534120.1:n.35-1746T>G
XM_011535818.3:c.35-1746T>G XP_011534120.1:n.35-1746T>G