Canonical Allele Identifier: CA31347157

Gene: ACKR1

Linked Data

• dbSNP Id: rs148618850
• gnomAD v2: 1-159175538-T-A
• gnomAD v3: 1-159205748-T-A
• gnomAD v4: 1-159205748-T-A
• MyVariant Identifiers: chr1:g.159175538T>A (hg19) ; chr1:g.159205748T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159205748T>A , CM000663.2:g.159205748T>A	GRCh38
NC_000001.10:g.159175538T>A , CM000663.1:g.159175538T>A	GRCh37
NC_000001.9:g.157442162T>A	NCBI36
NG_011626.1:g.6029T>A
NG_011626.3:g.6736T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368121.6:c.315T>A	ENSP00000357103.2:p.Ala105=
ENST00000368122.4:c.309T>A MANE Select	ENSP00000357104.1:p.Ala103=
ENST00000435307.2:n.490T>A
ENST00000368121.3:c.315T>A	ENSP00000357103.2:p.Ala105=
ENST00000368122.2:c.309T>A	ENSP00000357104.1:p.Ala103=
ENST00000435307.1:c.315T>A	ENSP00000398406.1:p.Ala105=
ENST00000537147.5:c.309T>A	ENSP00000441985.1:p.Ala103=
NM_001122951.2:c.315T>A	NP_001116423.1:p.Ala105=
NM_002036.3:c.309T>A	NP_002027.2:p.Ala103=
NM_002036.4:c.309T>A MANE Select	NP_002027.2:p.Ala103=
NM_001122951.3:c.315T>A	NP_001116423.1:p.Ala105=