Canonical Allele Identifier: CA619226133

Gene: IREB2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78450034G>T , CM000677.2:g.78450034G>T	GRCh38
NC_000015.9:g.78742376G>T , CM000677.1:g.78742376G>T	GRCh37
NC_000015.8:g.76529431G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258886.13:c.106+10153G>T MANE Select	ENSP00000258886.8:n.106+10153G>T
ENST00000258886.12:c.106+10153G>T	ENSP00000258886.8:n.106+10153G>T
ENST00000558525.5:c.101+10158G>T	ENSP00000453058.1:n.101+10158G>T
ENST00000558570.5:c.106+10153G>T	ENSP00000454063.1:n.106+10153G>T
ENST00000559215.5:c.106+10153G>T	ENSP00000453532.1:n.106+10153G>T
ENST00000560440.5:c.106+10153G>T	ENSP00000452938.1:n.106+10153G>T
ENST00000560454.1:n.522+10153G>T
ENST00000560840.5:c.-66+10153G>T	ENSP00000453172.1:n.-66+10153G>T
NM_004136.2:c.106+10153G>T	NP_004127.1:n.106+10153G>T
NM_001320941.1:c.-575+10153G>T	NP_001307870.1:n.-575+10153G>T
NM_001320942.1:c.-66+10153G>T	NP_001307871.1:n.-66+10153G>T
NM_001320943.1:c.106+10153G>T	NP_001307872.1:n.106+10153G>T
NM_001354994.1:c.-66+10153G>T	NP_001341923.1:n.-66+10153G>T
NM_004136.3:c.106+10153G>T	NP_004127.1:n.106+10153G>T
NM_004136.4:c.106+10153G>T MANE Select	NP_004127.2:n.106+10153G>T
NM_001320941.2:c.-575+10153G>T	NP_001307870.2:n.-575+10153G>T
NM_001320942.2:c.-66+10153G>T	NP_001307871.2:n.-66+10153G>T
NM_001320943.2:c.106+10153G>T	NP_001307872.1:n.106+10153G>T
NM_001354994.2:c.-66+10153G>T	NP_001341923.2:n.-66+10153G>T