Canonical Allele Identifier: CA2483456458

Gene: CR1

Linked Data

• dbSNP Id: rs1661928988

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611525T>C , CM000663.2:g.207611525T>C	GRCh38
NC_000001.10:g.207784870T>C , CM000663.1:g.207784870T>C	GRCh37
NC_000001.9:g.205851493T>C	NCBI36
NG_007481.1:g.120398T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367049.9:c.6296-152T>C MANE Select	ENSP00000356016.4:n.6296-152T>C
ENST00000367051.6:c.4946-152T>C	ENSP00000356018.1:n.4946-152T>C
ENST00000367052.6:c.4946-152T>C	ENSP00000356019.1:n.4946-152T>C
ENST00000367053.6:c.4946-152T>C	ENSP00000356020.1:n.4946-152T>C
ENST00000400960.7:c.4946-152T>C	ENSP00000383744.2:n.4946-152T>C
ENST00000367049.8:c.6296-152T>C	ENSP00000356016.4:n.6296-152T>C
ENST00000367051.5:c.4946-152T>C	ENSP00000356018.1:n.4946-152T>C
ENST00000367052.5:c.4946-152T>C	ENSP00000356019.1:n.4946-152T>C
ENST00000367053.5:c.4946-152T>C	ENSP00000356020.1:n.4946-152T>C
ENST00000400960.6:c.4946-152T>C	ENSP00000383744.2:n.4946-152T>C
ENST00000529814.1:c.1180-5050T>C
NM_000573.3:c.4946-152T>C	NP_000564.2:n.4946-152T>C
NM_000651.4:c.6296-152T>C	NP_000642.3:n.6296-152T>C
XM_006711166.2:c.6311-152T>C	XP_006711229.1:n.6311-152T>C
XM_011509205.1:c.6311-152T>C	XP_011507507.1:n.6311-152T>C
NM_000651.5:c.6296-152T>C	NP_000642.3:n.6296-152T>C
XM_024453287.1:c.4961-152T>C	XP_024309055.1:n.4961-152T>C
NM_000573.4:c.4946-152T>C	NP_000564.2:n.4946-152T>C
NM_000651.6:c.6296-152T>C MANE Select	NP_000642.3:n.6296-152T>C