Canonical Allele Identifier: CA344545136

Gene: CR1

Linked Data

• dbSNP Id: rs1661937194
• gnomAD v4: 1-207611776-G-C
• MyVariant Identifiers: chr1:g.207785121G>C (hg19) ; chr1:g.207611776G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611776G>C , CM000663.2:g.207611776G>C	GRCh38
NC_000001.10:g.207785121G>C , CM000663.1:g.207785121G>C	GRCh37
NC_000001.9:g.205851744G>C	NCBI36
NG_007481.1:g.120649G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6395G>C MANE Select	ENSP00000356016.4:p.Ser2132Thr
ENST00000367051.6:c.5045G>C	ENSP00000356018.1:p.Ser1682Thr
ENST00000367052.6:c.5045G>C	ENSP00000356019.1:p.Ser1682Thr
ENST00000367053.6:c.5045G>C	ENSP00000356020.1:p.Ser1682Thr
ENST00000400960.7:c.5045G>C	ENSP00000383744.2:p.Ser1682Thr
ENST00000367049.8:c.6395G>C	ENSP00000356016.4:p.Ser2132Thr
ENST00000367051.5:c.5045G>C	ENSP00000356018.1:p.Ser1682Thr
ENST00000367052.5:c.5045G>C	ENSP00000356019.1:p.Ser1682Thr
ENST00000367053.5:c.5045G>C	ENSP00000356020.1:p.Ser1682Thr
ENST00000400960.6:c.5045G>C	ENSP00000383744.2:p.Ser1682Thr
ENST00000529814.1:c.1180-4799G>C
NM_000573.3:c.5045G>C	NP_000564.2:p.Ser1682Thr
NM_000651.4:c.6395G>C	NP_000642.3:p.Ser2132Thr
XM_006711166.2:c.6410G>C	XP_006711229.1:p.Ser2137Thr
XM_011509205.1:c.6410G>C	XP_011507507.1:p.Ser2137Thr
NM_000651.5:c.6395G>C	NP_000642.3:p.Ser2132Thr
XM_024453287.1:c.5060G>C	XP_024309055.1:p.Ser1687Thr
NM_000573.4:c.5045G>C	NP_000564.2:p.Ser1682Thr
NM_000651.6:c.6395G>C MANE Select	NP_000642.3:p.Ser2132Thr