Canonical Allele Identifier: CA683311506

Gene: CMKLR1

Linked Data

• dbSNP Id: rs11113818
• MyVariant Identifiers: chr12:g.108717929C>A (hg19) ; chr12:g.108324152C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108324152C>A , CM000674.2:g.108324152C>A	GRCh38
NC_000012.11:g.108717929C>A , CM000674.1:g.108717929C>A	GRCh37
NC_000012.10:g.107242059C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000550402.6:c.-74+5843G>T MANE Select	ENSP00000449716.1:n.-74+5843G>T
ENST00000312143.11:c.-74+14875G>T	ENSP00000311733.7:n.-74+14875G>T
ENST00000550402.5:c.-74+5843G>T	ENSP00000449716.1:n.-74+5843G>T
ENST00000552995.5:c.-4+5843G>T	ENSP00000447579.1:n.-4+5843G>T
NM_001142343.1:c.-74+5843G>T	NP_001135815.1:n.-74+5843G>T
NM_001142344.1:c.-74+14875G>T	NP_001135816.1:n.-74+14875G>T
NM_004072.2:c.-4+5843G>T	NP_004063.1:n.-4+5843G>T
XM_017018820.2:c.-4+14875G>T	XP_016874309.1:n.-4+14875G>T
NM_001142343.2:c.-74+5843G>T MANE Select	NP_001135815.1:n.-74+5843G>T
NM_001142344.2:c.-74+14875G>T	NP_001135816.1:n.-74+14875G>T
NM_004072.3:c.-4+5843G>T	NP_004063.1:n.-4+5843G>T