Canonical Allele Identifier: CA715967409

Gene: IREB2

Linked Data

• dbSNP Id: rs1393922621
• MyVariant Identifiers: chr15:g.78792542G>C (hg19) ; chr15:g.78500200G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78500200G>C , CM000677.2:g.78500200G>C	GRCh38
NC_000015.9:g.78792542G>C , CM000677.1:g.78792542G>C	GRCh37
NC_000015.8:g.76579597G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000258886.13:c.*2057G>C MANE Select	ENSP00000258886.8:n.*2057G>C
ENST00000258886.12:c.*2057G>C	ENSP00000258886.8:n.*2057G>C
NM_004136.2:c.*2057G>C	NP_004127.1:n.*2057G>C
NM_001320941.1:c.*2057G>C	NP_001307870.1:n.*2057G>C
NM_001320942.1:c.*2057G>C	NP_001307871.1:n.*2057G>C
NM_001354994.1:c.*2057G>C	NP_001341923.1:n.*2057G>C
NM_004136.3:c.*2057G>C	NP_004127.1:n.*2057G>C
NM_004136.4:c.*2057G>C MANE Select	NP_004127.2:n.*2057G>C
NM_001320941.2:c.*2057G>C	NP_001307870.2:n.*2057G>C
NM_001320942.2:c.*2057G>C	NP_001307871.2:n.*2057G>C
NM_001354994.2:c.*2057G>C	NP_001341923.2:n.*2057G>C