Canonical Allele Identifier: CA344545002
Gene: CR1 HGNC NCBI

Linked Data

dbSNP Id: rs1205844405

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207611716C>T , CM000663.2:g.207611716C>T GRCh38
NC_000001.10:g.207785061C>T , CM000663.1:g.207785061C>T GRCh37
NC_000001.9:g.205851684C>T NCBI36
NG_007481.1:g.120589C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367049.9:c.6335C>T MANE Select ENSP00000356016.4:p.Thr2112Ile
ENST00000367051.6:c.4985C>T ENSP00000356018.1:p.Thr1662Ile
ENST00000367052.6:c.4985C>T ENSP00000356019.1:p.Thr1662Ile
ENST00000367053.6:c.4985C>T ENSP00000356020.1:p.Thr1662Ile
ENST00000400960.7:c.4985C>T ENSP00000383744.2:p.Thr1662Ile
ENST00000367049.8:c.6335C>T ENSP00000356016.4:p.Thr2112Ile
ENST00000367051.5:c.4985C>T ENSP00000356018.1:p.Thr1662Ile
ENST00000367052.5:c.4985C>T ENSP00000356019.1:p.Thr1662Ile
ENST00000367053.5:c.4985C>T ENSP00000356020.1:p.Thr1662Ile
ENST00000400960.6:c.4985C>T ENSP00000383744.2:p.Thr1662Ile
ENST00000529814.1:c.1180-4859C>T
NM_000573.3:c.4985C>T NP_000564.2:p.Thr1662Ile
NM_000651.4:c.6335C>T NP_000642.3:p.Thr2112Ile
XM_006711166.2:c.6350C>T XP_006711229.1:p.Thr2117Ile
XM_011509205.1:c.6350C>T XP_011507507.1:p.Thr2117Ile
NM_000651.5:c.6335C>T NP_000642.3:p.Thr2112Ile
XM_024453287.1:c.5000C>T XP_024309055.1:p.Thr1667Ile
NM_000573.4:c.4985C>T NP_000564.2:p.Thr1662Ile
NM_000651.6:c.6335C>T MANE Select NP_000642.3:p.Thr2112Ile