Canonical Allele Identifier: CA770871022

Gene: BCL11A

Linked Data

• dbSNP Id: rs531398346
• gnomAD v3: 2-60493152-G-A
• gnomAD v4: 2-60493152-G-A
• MyVariant Identifiers: chr2:g.60720287G>A (hg19) ; chr2:g.60493152G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.60493152G>A , CM000664.2:g.60493152G>A	GRCh38
NC_000002.11:g.60720287G>A , CM000664.1:g.60720287G>A	GRCh37
NC_000002.10:g.60573791G>A	NCBI36
NG_011968.1:g.65347C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000335712.11:c.386-30728C>T	ENSP00000338774.7:n.386-30728C>T
ENST00000356842.9:c.386-24319C>T	ENSP00000349300.4:n.386-24319C>T
ENST00000358510.6:c.386-30728C>T	ENSP00000351307.5:n.386-30728C>T
ENST00000359629.10:c.386-24319C>T	ENSP00000352648.5:n.386-24319C>T
ENST00000489516.7:c.380-24319C>T	ENSP00000488390.2:n.380-24319C>T
ENST00000492272.6:n.228-24319C>T
ENST00000642384.2:c.386-24319C>T MANE Select	ENSP00000496168.1:n.386-24319C>T
ENST00000642439.1:c.386-30728C>T	ENSP00000493484.1:n.386-30728C>T
ENST00000643222.1:c.371-30728C>T	ENSP00000495862.1:n.371-30728C>T
ENST00000643459.1:c.371-24319C>T	ENSP00000494996.1:n.371-24319C>T
ENST00000644606.1:n.425-24319C>T
ENST00000645455.1:n.202-24319C>T
ENST00000646249.1:c.386-30728C>T	ENSP00000495759.1:n.386-30728C>T
ENST00000647472.1:c.232-14913C>T
ENST00000335712.10:c.386-24319C>T	ENSP00000338774.6:n.386-24319C>T
ENST00000356842.8:c.386-24319C>T	ENSP00000349300.4:n.386-24319C>T
ENST00000358510.5:c.386-30728C>T	ENSP00000351307.4:n.386-30728C>T
ENST00000359629.9:c.386-24319C>T	ENSP00000352648.5:n.386-24319C>T
ENST00000477659.1:n.69-24319C>T
ENST00000489516.6:c.230-24319C>T	ENSP00000488390.1:n.230-24319C>T
ENST00000492272.5:n.228-24319C>T
ENST00000631857.1:c.*100+15454C>T	ENSP00000488886.1:n.*100+15454C>T
NM_018014.3:c.386-24319C>T	NP_060484.2:n.386-24319C>T
NM_022893.3:c.386-24319C>T	NP_075044.2:n.386-24319C>T
NM_138559.1:c.386-24319C>T	NP_612569.1:n.386-24319C>T
XM_011532909.1:c.386-24319C>T	XP_011531211.1:n.386-24319C>T
XM_011532910.1:c.386-24319C>T	XP_011531212.1:n.386-24319C>T
XM_011532911.1:c.386-30728C>T	XP_011531213.1:n.386-30728C>T
XM_011532912.1:c.386-30728C>T	XP_011531214.1:n.386-30728C>T
XM_011532913.1:c.380-24319C>T	XP_011531215.1:n.380-24319C>T
XM_011532914.1:c.380-30728C>T	XP_011531216.1:n.380-30728C>T
XM_011532915.1:c.52+23275C>T	XP_011531217.1:n.52+23275C>T
NM_001363864.1:c.386-30728C>T	NP_001350793.1:n.386-30728C>T
NM_001365609.1:c.386-30728C>T	NP_001352538.1:n.386-30728C>T
XM_017004333.1:c.380-24319C>T	XP_016859822.1:n.380-24319C>T
XM_017004335.1:c.380-30728C>T	XP_016859824.1:n.380-30728C>T
XM_017004336.1:c.52+23275C>T	XP_016859825.1:n.52+23275C>T
XM_024452962.1:c.230-24319C>T	XP_024308730.1:n.230-24319C>T
XM_024452963.1:c.230-24319C>T	XP_024308731.1:n.230-24319C>T
NM_018014.4:c.386-24319C>T	NP_060484.2:n.386-24319C>T
NM_022893.4:c.386-24319C>T MANE Select	NP_075044.2:n.386-24319C>T
NM_138559.2:c.386-24319C>T	NP_612569.1:n.386-24319C>T