Canonical Allele Identifier: CA49056409

Gene: REL

Linked Data

• dbSNP Id: rs139184566
• gnomAD v3: 2-60897710-C-T
• gnomAD v4: 2-60897710-C-T
• MyVariant Identifiers: chr2:g.61124845C>T (hg19) ; chr2:g.60897710C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.60897710C>T , CM000664.2:g.60897710C>T	GRCh38
NC_000002.11:g.61124845C>T , CM000664.1:g.61124845C>T	GRCh37
NC_000002.10:g.60978349C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699191.1:c.302+3165C>T	ENSP00000514191.1:n.302+3165C>T
ENST00000699192.1:c.302+3165C>T	ENSP00000514192.1:n.302+3165C>T
ENST00000699193.1:c.302+3165C>T	ENSP00000514193.1:n.302+3165C>T
ENST00000699194.1:n.253+3165C>T
ENST00000394479.4:c.302+3165C>T MANE Select	ENSP00000377989.4:n.302+3165C>T
ENST00000642725.1:c.150-1260C>T	ENSP00000496299.1:n.150-1260C>T
ENST00000295025.12:c.302+3165C>T	ENSP00000295025.7:n.302+3165C>T
ENST00000394479.3:c.302+3165C>T	ENSP00000377989.3:n.302+3165C>T
NM_001291746.1:c.302+3165C>T	NP_001278675.1:n.302+3165C>T
NM_002908.3:c.302+3165C>T	NP_002899.1:n.302+3165C>T
XM_017004627.2:c.302+3165C>T	XP_016860116.1:n.302+3165C>T
NM_001291746.2:c.302+3165C>T MANE Select	NP_001278675.1:n.302+3165C>T
NM_002908.4:c.302+3165C>T	NP_002899.1:n.302+3165C>T