Canonical Allele Identifier: CA145437951

Gene: LIN28B

Linked Data

• MyVariant Identifiers: chr6:g.105443841_105443842insTA (hg19) ; chr6:g.104995966_104995967insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104995966_104995967insTA , CM000668.2:g.104995966_104995967insTA	GRCh38
NC_000006.11:g.105443841_105443842insTA , CM000668.1:g.105443841_105443842insTA	GRCh37
NC_000006.10:g.105550534_105550535insTA	NCBI36
NG_032815.1:g.43919_43920insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345080.5:c.199-30332_199-30331insTA MANE Select	ENSP00000344401.4:n.199-30332_199-30331insTA
ENST00000635857.1:c.256-30332_256-30331insTA	ENSP00000489735.1:n.256-30332_256-30331insTA
ENST00000637759.1:c.223-30332_223-30331insTA	ENSP00000490468.1:n.223-30332_223-30331insTA
ENST00000345080.4:c.199-30332_199-30331insTA	ENSP00000344401.4:n.199-30332_199-30331insTA
NM_001004317.3:c.199-30332_199-30331insTA	NP_001004317.1:n.199-30332_199-30331insTA
XM_006715477.2:c.256-30332_256-30331insTA	XP_006715540.2:n.256-30332_256-30331insTA
XM_011535818.1:c.223-30332_223-30331insTA	XP_011534120.1:n.223-30332_223-30331insTA
XM_011535818.3:c.223-30332_223-30331insTA	XP_011534120.1:n.223-30332_223-30331insTA
NM_001004317.4:c.199-30332_199-30331insTA MANE Select	NP_001004317.1:n.199-30332_199-30331insTA