Canonical Allele Identifier: CA10740559
Gene: ACKR1 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.159204333C>T
GRCh37 chr1:g.159174123C>T
gnomAD v2:
1:159174123 C / T
gnomAD v3:
1:159204333 C / T
gnomAD v4:
chr1-159204333-C-T
Joint Max Group AF 0.1998605 (AMR)
Genomes Max Group AF 0.20204735 (AMR)
Exomes Max Group AF 0.15669638 (AMR)
dbSNP:
3027012
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159204333C>T , CM000663.2:g.159204333C>T GRCh38
NC_000001.10:g.159174123C>T , CM000663.1:g.159174123C>T GRCh37
NC_000001.9:g.157440747C>T NCBI36
NG_011626.1:g.4614C>T
NG_011626.3:g.5321C>T
NG_051933.1:g.37770C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368122.2:c.-627C>T ENSP00000357104.1:n.-627C>T
ENST00000537147.5:c.-627C>T ENSP00000441985.1:n.-627C>T
NM_002036.3:c.-627C>T NP_002027.2:n.-627C>T
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