Canonical Allele Identifier: CA816663085
Gene: LIN28B HGNC NCBI

Linked Data

dbSNP Id: rs1479831156
MyVariant Identifiers: chr6:g.105443972T>A (hg19) chr6:g.104996097T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104996097T>A , CM000668.2:g.104996097T>A GRCh38
NC_000006.11:g.105443972T>A , CM000668.1:g.105443972T>A GRCh37
NC_000006.10:g.105550665T>A NCBI36
NG_032815.1:g.44050T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000345080.5:c.199-30201T>A MANE Select ENSP00000344401.4:n.199-30201T>A
ENST00000635857.1:c.256-30201T>A ENSP00000489735.1:n.256-30201T>A
ENST00000637759.1:c.223-30201T>A ENSP00000490468.1:n.223-30201T>A
ENST00000345080.4:c.199-30201T>A ENSP00000344401.4:n.199-30201T>A
NM_001004317.3:c.199-30201T>A NP_001004317.1:n.199-30201T>A
XM_006715477.2:c.256-30201T>A XP_006715540.2:n.256-30201T>A
XM_011535818.1:c.223-30201T>A XP_011534120.1:n.223-30201T>A
XM_011535818.3:c.223-30201T>A XP_011534120.1:n.223-30201T>A
NM_001004317.4:c.199-30201T>A MANE Select NP_001004317.1:n.199-30201T>A
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