Canonical Allele Identifier: CA423139748

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207475146T>C , CM000663.2:g.207475146T>C	GRCh38
NC_000001.10:g.207648491T>C , CM000663.1:g.207648491T>C	GRCh37
NC_000001.9:g.205715114T>C	NCBI36
NG_013006.1:g.25847T>C , LRG_348:g.25847T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.2100T>C	ENSP00000514480.1:p.Asn700=
ENST00000699621.1:c.2089T>C
ENST00000367057.8:c.2646T>C MANE Select	ENSP00000356024.3:p.Asn882=
ENST00000367057.7:c.2646T>C	ENSP00000356024.3:p.Asn882=
ENST00000367058.7:c.2469T>C	ENSP00000356025.3:p.Asn823=
ENST00000367059.3:c.2469T>C	ENSP00000356026.3:p.Asn823=
NM_001006658.2:c.2646T>C , LRG_348t1:c.2646T>C	NP_001006659.1:p.Asn882=
NM_001877.4:c.2469T>C	NP_001868.2:p.Asn823=
XM_011509206.1:c.2277T>C	XP_011507508.1:p.Asn759=
XM_011509206.3:c.2277T>C	XP_011507508.1:p.Asn759=
NM_001006658.3:c.2646T>C MANE Select	NP_001006659.1:p.Asn882=
NM_001877.5:c.2469T>C	NP_001868.2:p.Asn823=