Canonical Allele Identifier: CA1394098691

Gene: CD200R1

Linked Data

• dbSNP Id: rs1488193

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112962738A>C , CM000665.2:g.112962738A>C	GRCh38
NC_000003.11:g.112681585A>C , CM000665.1:g.112681585A>C	GRCh37
NC_000003.10:g.114164275A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000308611.8:c.67+12053T>G MANE Select	ENSP00000311035.3:n.67+12053T>G
ENST00000295863.4:c.67+12053T>G	ENSP00000295863.4:n.67+12053T>G
ENST00000308611.7:c.67+12053T>G	ENSP00000311035.3:n.67+12053T>G
ENST00000440122.6:c.67+12053T>G	ENSP00000405733.2:n.67+12053T>G
ENST00000471858.5:c.67+12053T>G	ENSP00000418928.1:n.67+12053T>G
ENST00000490004.1:c.67+12053T>G	ENSP00000418801.1:n.67+12053T>G
NM_138806.3:c.67+12053T>G	NP_620161.1:n.67+12053T>G
NM_138939.2:c.67+12053T>G	NP_620385.1:n.67+12053T>G
NM_138940.2:c.67+12053T>G	NP_620386.1:n.67+12053T>G
NM_170780.2:c.67+12053T>G	NP_740750.1:n.67+12053T>G
XM_006713492.2:c.67+12053T>G	XP_006713555.1:n.67+12053T>G
NM_138806.4:c.67+12053T>G MANE Select	NP_620161.1:n.67+12053T>G
NM_138939.3:c.67+12053T>G	NP_620385.1:n.67+12053T>G
NM_138940.3:c.67+12053T>G	NP_620386.1:n.67+12053T>G
NM_170780.3:c.67+12053T>G	NP_740750.1:n.67+12053T>G