Canonical Allele Identifier: CA422972817

Gene: CR1

Linked Data

• dbSNP Id: rs1445837706
• gnomAD v2: 1-207785071-T-C
• gnomAD v4: 1-207611726-T-C
• MyVariant Identifiers: chr1:g.207785071T>C (hg19) ; chr1:g.207611726T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611726T>C , CM000663.2:g.207611726T>C	GRCh38
NC_000001.10:g.207785071T>C , CM000663.1:g.207785071T>C	GRCh37
NC_000001.9:g.205851694T>C	NCBI36
NG_007481.1:g.120599T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6345T>C MANE Select	ENSP00000356016.4:p.His2115=
ENST00000367051.6:c.4995T>C	ENSP00000356018.1:p.His1665=
ENST00000367052.6:c.4995T>C	ENSP00000356019.1:p.His1665=
ENST00000367053.6:c.4995T>C	ENSP00000356020.1:p.His1665=
ENST00000400960.7:c.4995T>C	ENSP00000383744.2:p.His1665=
ENST00000367049.8:c.6345T>C	ENSP00000356016.4:p.His2115=
ENST00000367051.5:c.4995T>C	ENSP00000356018.1:p.His1665=
ENST00000367052.5:c.4995T>C	ENSP00000356019.1:p.His1665=
ENST00000367053.5:c.4995T>C	ENSP00000356020.1:p.His1665=
ENST00000400960.6:c.4995T>C	ENSP00000383744.2:p.His1665=
ENST00000529814.1:c.1180-4849T>C
NM_000573.3:c.4995T>C	NP_000564.2:p.His1665=
NM_000651.4:c.6345T>C	NP_000642.3:p.His2115=
XM_006711166.2:c.6360T>C	XP_006711229.1:p.His2120=
XM_011509205.1:c.6360T>C	XP_011507507.1:p.His2120=
NM_000651.5:c.6345T>C	NP_000642.3:p.His2115=
XM_024453287.1:c.5010T>C	XP_024309055.1:p.His1670=
NM_000573.4:c.4995T>C	NP_000564.2:p.His1665=
NM_000651.6:c.6345T>C MANE Select	NP_000642.3:p.His2115=