Canonical Allele Identifier: CA15836005
Gene: IREB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78441389T>C , CM000677.2:g.78441389T>C GRCh38
NC_000015.9:g.78733731T>C , CM000677.1:g.78733731T>C GRCh37
NC_000015.8:g.76520786T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000258886.13:c.106+1508T>C MANE Select ENSP00000258886.8:n.106+1508T>C
ENST00000258886.12:c.106+1508T>C ENSP00000258886.8:n.106+1508T>C
ENST00000558525.5:c.101+1513T>C ENSP00000453058.1:n.101+1513T>C
ENST00000558570.5:c.106+1508T>C ENSP00000454063.1:n.106+1508T>C
ENST00000559215.5:c.106+1508T>C ENSP00000453532.1:n.106+1508T>C
ENST00000560440.5:c.106+1508T>C ENSP00000452938.1:n.106+1508T>C
ENST00000560454.1:n.522+1508T>C
ENST00000560840.5:c.-66+1508T>C ENSP00000453172.1:n.-66+1508T>C
NM_004136.2:c.106+1508T>C NP_004127.1:n.106+1508T>C
NM_001320941.1:c.-575+1508T>C NP_001307870.1:n.-575+1508T>C
NM_001320942.1:c.-66+1508T>C NP_001307871.1:n.-66+1508T>C
NM_001320943.1:c.106+1508T>C NP_001307872.1:n.106+1508T>C
NM_001354994.1:c.-66+1508T>C NP_001341923.1:n.-66+1508T>C
NM_004136.3:c.106+1508T>C NP_004127.1:n.106+1508T>C
NM_004136.4:c.106+1508T>C MANE Select NP_004127.2:n.106+1508T>C
NM_001320941.2:c.-575+1508T>C NP_001307870.2:n.-575+1508T>C
NM_001320942.2:c.-66+1508T>C NP_001307871.2:n.-66+1508T>C
NM_001320943.2:c.106+1508T>C NP_001307872.1:n.106+1508T>C
NM_001354994.2:c.-66+1508T>C NP_001341923.2:n.-66+1508T>C
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