Canonical Allele Identifier: CA26518507

Gene: GTF2B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.88873739C>T , CM000663.2:g.88873739C>T	GRCh38
NC_000001.10:g.89339422C>T , CM000663.1:g.89339422C>T	GRCh37
NC_000001.9:g.89112010C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370500.10:c.125-9625G>A MANE Select	ENSP00000359531.5:n.125-9625G>A
ENST00000370500.9:c.125-9625G>A	ENSP00000359531.5:n.125-9625G>A
ENST00000418217.1:c.110-9625G>A	ENSP00000402345.1:n.110-9625G>A
ENST00000448623.5:c.122-9625G>A	ENSP00000415741.1:n.122-9625G>A
ENST00000471296.5:n.465-9625G>A
ENST00000471471.1:n.446-9625G>A
ENST00000486078.1:n.164-9625G>A
ENST00000494819.5:n.153-9625G>A
NM_001514.5:c.125-9625G>A	NP_001505.1:n.125-9625G>A
XM_011541299.1:c.32-9625G>A	XP_011539601.1:n.32-9625G>A
XR_946615.1:n.191-9625G>A
XR_001737129.1:n.191-9625G>A
NM_001514.6:c.125-9625G>A MANE Select	NP_001505.1:n.125-9625G>A