Canonical Allele Identifier: CA145437942
Gene: LIN28B HGNC NCBI

Linked Data

dbSNP Id: rs933094933
MyVariant Identifiers: chr6:g.105443780A>C (hg19) chr6:g.104995905A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104995905A>C , CM000668.2:g.104995905A>C GRCh38
NC_000006.11:g.105443780A>C , CM000668.1:g.105443780A>C GRCh37
NC_000006.10:g.105550473A>C NCBI36
NG_032815.1:g.43858A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000345080.5:c.199-30393A>C MANE Select ENSP00000344401.4:n.199-30393A>C
ENST00000635857.1:c.256-30393A>C ENSP00000489735.1:n.256-30393A>C
ENST00000637759.1:c.223-30393A>C ENSP00000490468.1:n.223-30393A>C
ENST00000345080.4:c.199-30393A>C ENSP00000344401.4:n.199-30393A>C
NM_001004317.3:c.199-30393A>C NP_001004317.1:n.199-30393A>C
XM_006715477.2:c.256-30393A>C XP_006715540.2:n.256-30393A>C
XM_011535818.1:c.223-30393A>C XP_011534120.1:n.223-30393A>C
XM_011535818.3:c.223-30393A>C XP_011534120.1:n.223-30393A>C
NM_001004317.4:c.199-30393A>C MANE Select NP_001004317.1:n.199-30393A>C
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