Canonical Allele Identifier: CA145433653
Gene: LIN28B HGNC NCBI

Linked Data

dbSNP Id: rs972204336
gnomAD v3: 6-104956326-G-A
gnomAD v4: 6-104956326-G-A
MyVariant Identifiers: chr6:g.105404201G>A (hg19) chr6:g.104956326G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104956326G>A , CM000668.2:g.104956326G>A GRCh38
NC_000006.11:g.105404201G>A , CM000668.1:g.105404201G>A GRCh37
NC_000006.10:g.105510894G>A NCBI36
NG_032815.1:g.4279G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000635857.1:c.68-1773G>A ENSP00000489735.1:n.68-1773G>A
ENST00000637759.1:c.35-1773G>A ENSP00000490468.1:n.35-1773G>A
XM_006715477.2:c.68-1773G>A XP_006715540.2:n.68-1773G>A
XM_011535818.1:c.35-1773G>A XP_011534120.1:n.35-1773G>A
XM_011535818.3:c.35-1773G>A XP_011534120.1:n.35-1773G>A
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