Canonical Allele Identifier: CA2629776889

Gene: IREB2

Linked Data

• gnomAD v4: 15-78500192-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78500192A>G , CM000677.2:g.78500192A>G	GRCh38
NC_000015.9:g.78792534A>G , CM000677.1:g.78792534A>G	GRCh37
NC_000015.8:g.76579589A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000258886.13:c.*2049A>G MANE Select	ENSP00000258886.8:n.*2049A>G
ENST00000258886.12:c.*2049A>G	ENSP00000258886.8:n.*2049A>G
NM_004136.2:c.*2049A>G	NP_004127.1:n.*2049A>G
NM_001320941.1:c.*2049A>G	NP_001307870.1:n.*2049A>G
NM_001320942.1:c.*2049A>G	NP_001307871.1:n.*2049A>G
NM_001354994.1:c.*2049A>G	NP_001341923.1:n.*2049A>G
NM_004136.3:c.*2049A>G	NP_004127.1:n.*2049A>G
NM_004136.4:c.*2049A>G MANE Select	NP_004127.2:n.*2049A>G
NM_001320941.2:c.*2049A>G	NP_001307870.2:n.*2049A>G
NM_001320942.2:c.*2049A>G	NP_001307871.2:n.*2049A>G
NM_001354994.2:c.*2049A>G	NP_001341923.2:n.*2049A>G