Canonical Allele Identifier: CA816644157
Gene: LIN28B HGNC NCBI

Linked Data

dbSNP Id: rs1364721051
MyVariant Identifiers: chr6:g.105404199C>T (hg19) chr6:g.104956324C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104956324C>T , CM000668.2:g.104956324C>T GRCh38
NC_000006.11:g.105404199C>T , CM000668.1:g.105404199C>T GRCh37
NC_000006.10:g.105510892C>T NCBI36
NG_032815.1:g.4277C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000635857.1:c.68-1775C>T ENSP00000489735.1:n.68-1775C>T
ENST00000637759.1:c.35-1775C>T ENSP00000490468.1:n.35-1775C>T
XM_006715477.2:c.68-1775C>T XP_006715540.2:n.68-1775C>T
XM_011535818.1:c.35-1775C>T XP_011534120.1:n.35-1775C>T
XM_011535818.3:c.35-1775C>T XP_011534120.1:n.35-1775C>T
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