Canonical Allele Identifier: CA12446746
Gene: LIN28B HGNC NCBI
dbSNP:
314263
gnomAD v2:
6:105392745 C / T
gnomAD v3:
6:104944870 C / T
gnomAD v4:
chr6-104944870-C-T
Joint Max Group AF 0.71626097 (AMR)
Genomes Max Group AF 0.71626097 (AMR)
MyVariant.info:
GRCh38 chr6:g.104944870C>T
GRCh37 chr6:g.105392745C>T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104944870C>T , CM000668.2:g.104944870C>T GRCh38
NC_000006.11:g.105392745C>T , CM000668.1:g.105392745C>T GRCh37
NC_000006.10:g.105499438C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000635857.1:c.19-5591C>T ENSP00000489735.1:n.19-5591C>T
ENST00000637759.1:c.-16+3858C>T ENSP00000490468.1:n.-16+3858C>T
XM_006715477.2:c.19-5591C>T XP_006715540.2:n.19-5591C>T
XM_011535818.1:c.-16+3858C>T XP_011534120.1:n.-16+3858C>T
XM_011535818.3:c.-16+3858C>T XP_011534120.1:n.-16+3858C>T
Search 100 bp 5'
Search 100 bp 3'