Canonical Allele Identifier: CA2510748942
Gene: LIN28B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104996163A>C , CM000668.2:g.104996163A>C GRCh38
NC_000006.11:g.105444038A>C , CM000668.1:g.105444038A>C GRCh37
NC_000006.10:g.105550731A>C NCBI36
NG_032815.1:g.44116A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000345080.5:c.199-30135A>C MANE Select ENSP00000344401.4:n.199-30135A>C
ENST00000635857.1:c.256-30135A>C ENSP00000489735.1:n.256-30135A>C
ENST00000637759.1:c.223-30135A>C ENSP00000490468.1:n.223-30135A>C
ENST00000345080.4:c.199-30135A>C ENSP00000344401.4:n.199-30135A>C
NM_001004317.3:c.199-30135A>C NP_001004317.1:n.199-30135A>C
XM_006715477.2:c.256-30135A>C XP_006715540.2:n.256-30135A>C
XM_011535818.1:c.223-30135A>C XP_011534120.1:n.223-30135A>C
XM_011535818.3:c.223-30135A>C XP_011534120.1:n.223-30135A>C
NM_001004317.4:c.199-30135A>C MANE Select NP_001004317.1:n.199-30135A>C
Search 100 bp 5'
Search 100 bp 3'