Canonical Allele Identifier: CA113788
Gene: ACKR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 18395
ClinVar RCV Id: RCV000000006 RCV000000007 RCV000000008
dbSNP Id: rs2814778
gnomAD v2: 1-159174683-T-C
gnomAD v3: 1-159204893-T-C
gnomAD v4: 1-159204893-T-C
MyVariant Identifiers: chr1:g.159174683T>C (hg19) chr1:g.159204893T>C (hg38)
PubMed: PMID:7663520 PMID:8547665 PMID:8651934 PMID:10570183 PMID:10791881 PMID:17304246 PMID:18179887 PMID:18621010 PMID:19180233 PMID:19620399 PMID:20932074
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159204893T>C , CM000663.2:g.159204893T>C GRCh38
NC_000001.10:g.159174683T>C , CM000663.1:g.159174683T>C GRCh37
NC_000001.9:g.157441307T>C NCBI36
NG_011626.1:g.5174T>C
NG_011626.3:g.5881T>C
NG_051933.1:g.38330T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000368121.6:c.-111T>C ENSP00000357103.2:n.-111T>C
ENST00000368122.4:c.-67T>C MANE Select ENSP00000357104.1:n.-67T>C
ENST00000368122.2:c.-67T>C ENSP00000357104.1:n.-67T>C
ENST00000537147.5:c.-67T>C ENSP00000441985.1:n.-67T>C
NM_002036.3:c.-67T>C NP_002027.2:n.-67T>C
NM_002036.4:c.-67T>C MANE Select NP_002027.2:n.-67T>C
NM_001122951.3:c.-111T>C NP_001116423.1:n.-111T>C
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