Canonical Allele Identifier: CA919597161
Gene: IREB2 HGNC NCBI

Linked Data

dbSNP Id: rs1596021512

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78500191_78500196dup , CM000677.2:g.78500191_78500196dup GRCh38
NC_000015.9:g.78792533_78792538dup , CM000677.1:g.78792533_78792538dup GRCh37
NC_000015.8:g.76579588_76579593dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000258886.13:c.*2048_*2053dup MANE Select ENSP00000258886.8:n.*2048_*2053dup
ENST00000258886.12:c.*2048_*2053dup ENSP00000258886.8:n.*2048_*2053dup
NM_004136.2:c.*2048_*2053dup NP_004127.1:n.*2048_*2053dup
NM_001320941.1:c.*2048_*2053dup NP_001307870.1:n.*2048_*2053dup
NM_001320942.1:c.*2048_*2053dup NP_001307871.1:n.*2048_*2053dup
NM_001354994.1:c.*2048_*2053dup NP_001341923.1:n.*2048_*2053dup
NM_004136.3:c.*2048_*2053dup NP_004127.1:n.*2048_*2053dup
NM_004136.4:c.*2048_*2053dup MANE Select NP_004127.2:n.*2048_*2053dup
NM_001320941.2:c.*2048_*2053dup NP_001307870.2:n.*2048_*2053dup
NM_001320942.2:c.*2048_*2053dup NP_001307871.2:n.*2048_*2053dup
NM_001354994.2:c.*2048_*2053dup NP_001341923.2:n.*2048_*2053dup