Canonical Allele Identifier: CA565013943

Gene: IRF4

Linked Data

• dbSNP Id: rs1473407785
• gnomAD v2: 6-396396-C-T
• MyVariant Identifiers: chr6:g.396396C>T (hg19) ; chr6:g.396396C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396396C>T , CM000668.2:g.396396C>T	GRCh38
NC_000006.11:g.396396C>T , CM000668.1:g.396396C>T	GRCh37
NC_000006.10:g.341396C>T	NCBI36
NG_027728.1:g.9658C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000493114.2:c.492+461C>T	ENSP00000436094.2:n.492+461C>T
ENST00000696871.1:c.492+461C>T	ENSP00000512940.1:n.492+461C>T
ENST00000696872.1:c.552+461C>T	ENSP00000512941.1:n.552+461C>T
ENST00000696873.1:c.57+461C>T	ENSP00000512942.1:n.57+461C>T
ENST00000380956.9:c.492+461C>T MANE Select	ENSP00000370343.4:n.492+461C>T
ENST00000380956.8:c.492+461C>T	ENSP00000370343.4:n.492+461C>T
ENST00000493114.1:c.492+461C>T	ENSP00000436094.1:n.492+461C>T
ENST00000495137.5:n.318+461C>T
NM_001195286.1:c.492+461C>T	NP_001182215.1:n.492+461C>T
NM_002460.3:c.492+461C>T	NP_002451.2:n.492+461C>T
NR_046000.2:n.618+461C>T
XM_006715090.1:c.492+461C>T	XP_006715153.1:n.492+461C>T
XM_006715090.2:c.492+461C>T	XP_006715153.1:n.492+461C>T
NM_002460.4:c.492+461C>T MANE Select	NP_002451.2:n.492+461C>T
NM_001195286.2:c.492+461C>T	NP_001182215.1:n.492+461C>T
NR_046000.3:n.605+461C>T