Canonical Allele Identifier: CA1187701

Gene: ACKR1

Linked Data

• dbSNP Id: rs778208530
• ExAC: 1:159175539 G / A
• gnomAD v2: 1-159175539-G-A
• gnomAD v3: 1-159205749-G-A
• gnomAD v4: 1-159205749-G-A
• MyVariant Identifiers: chr1:g.159175539G>A (hg19) ; chr1:g.159205749G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159205749G>A , CM000663.2:g.159205749G>A	GRCh38
NC_000001.10:g.159175539G>A , CM000663.1:g.159175539G>A	GRCh37
NC_000001.9:g.157442163G>A	NCBI36
NG_011626.1:g.6030G>A
NG_011626.3:g.6737G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368121.6:c.316G>A	ENSP00000357103.2:p.Val106Met
ENST00000368122.4:c.310G>A MANE Select	ENSP00000357104.1:p.Val104Met
ENST00000435307.2:n.491G>A
ENST00000368121.3:c.316G>A	ENSP00000357103.2:p.Val106Met
ENST00000368122.2:c.310G>A	ENSP00000357104.1:p.Val104Met
ENST00000435307.1:c.316G>A	ENSP00000398406.1:p.Val106Met
ENST00000537147.5:c.310G>A	ENSP00000441985.1:p.Val104Met
NM_001122951.2:c.316G>A	NP_001116423.1:p.Val106Met
NM_002036.3:c.310G>A	NP_002027.2:p.Val104Met
NM_002036.4:c.310G>A MANE Select	NP_002027.2:p.Val104Met
NM_001122951.3:c.316G>A	NP_001116423.1:p.Val106Met