Canonical Allele Identifier: CA16275431
Gene: LIN28B HGNC NCBI

Linked Data

dbSNP Id: rs314279
gnomAD v2: 6-105402083-C-A
gnomAD v3: 6-104954208-C-A
gnomAD v4: 6-104954208-C-A
MyVariant Identifiers: chr6:g.105402083C>A (hg19) chr6:g.104954208C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104954208C>A , CM000668.2:g.104954208C>A GRCh38
NC_000006.11:g.105402083C>A , CM000668.1:g.105402083C>A GRCh37
NC_000006.10:g.105508776C>A NCBI36
NG_032815.1:g.2161C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000635857.1:c.67+3699C>A ENSP00000489735.1:n.67+3699C>A
ENST00000637759.1:c.34+3699C>A ENSP00000490468.1:n.34+3699C>A
XM_006715477.2:c.67+3699C>A XP_006715540.2:n.67+3699C>A
XM_011535818.1:c.34+3699C>A XP_011534120.1:n.34+3699C>A
XM_011535818.3:c.34+3699C>A XP_011534120.1:n.34+3699C>A
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