Canonical Allele Identifier: CA2581621047

Gene: LIN28B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104956323G>C , CM000668.2:g.104956323G>C	GRCh38
NC_000006.11:g.105404198G>C , CM000668.1:g.105404198G>C	GRCh37
NC_000006.10:g.105510891G>C	NCBI36
NG_032815.1:g.4276G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000635857.1:c.68-1776G>C	ENSP00000489735.1:n.68-1776G>C
ENST00000637759.1:c.35-1776G>C	ENSP00000490468.1:n.35-1776G>C
XM_006715477.2:c.68-1776G>C	XP_006715540.2:n.68-1776G>C
XM_011535818.1:c.35-1776G>C	XP_011534120.1:n.35-1776G>C
XM_011535818.3:c.35-1776G>C	XP_011534120.1:n.35-1776G>C