Canonical Allele Identifier: CA1187675

Gene: ACKR1

Linked Data

• ClinVar Variation Id: 1185002
• ClinVar RCV Id: RCV001543626
• dbSNP Id: rs118062001
• ExAC: 1:159175428 C / T
• gnomAD v2: 1-159175428-C-T
• gnomAD v3: 1-159205638-C-T
• gnomAD v4: 1-159205638-C-T
• MyVariant Identifiers: chr1:g.159175428C>T (hg19) ; chr1:g.159205638C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159205638C>T , CM000663.2:g.159205638C>T	GRCh38
NC_000001.10:g.159175428C>T , CM000663.1:g.159175428C>T	GRCh37
NC_000001.9:g.157442052C>T	NCBI36
NG_011626.1:g.5919C>T
NG_011626.3:g.6626C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368121.6:c.205C>T	ENSP00000357103.2:p.Leu69Phe
ENST00000368122.4:c.199C>T MANE Select	ENSP00000357104.1:p.Leu67Phe
ENST00000435307.2:n.380C>T
ENST00000368121.3:c.205C>T	ENSP00000357103.2:p.Leu69Phe
ENST00000368122.2:c.199C>T	ENSP00000357104.1:p.Leu67Phe
ENST00000435307.1:c.205C>T	ENSP00000398406.1:p.Leu69Phe
ENST00000537147.5:c.199C>T	ENSP00000441985.1:p.Leu67Phe
NM_001122951.2:c.205C>T	NP_001116423.1:p.Leu69Phe
NM_002036.3:c.199C>T	NP_002027.2:p.Leu67Phe
NM_002036.4:c.199C>T MANE Select	NP_002027.2:p.Leu67Phe
NM_001122951.3:c.205C>T	NP_001116423.1:p.Leu69Phe