Canonical Allele Identifier: CA351176471
Community Standard Title: NM_020311.3(ACKR3):c.772G>A (p.Val258Met)
Gene: ACKR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.236581237G>A , CM000664.2:g.236581237G>A GRCh38
NC_000002.11:g.237489880G>A , CM000664.1:g.237489880G>A GRCh37
NC_000002.10:g.237154619G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_020311.3:c.772G>A MANE Select NP_064707.1:p.Val258Met
ENST00000272928.4:c.772G>A MANE Select ENSP00000272928.3:p.Val258Met
NM_020311.2:c.772G>A NP_064707.1:p.Val258Met
ENST00000272928.3:c.772G>A ENSP00000272928.3:p.Val258Met
XM_005246097.1:c.772G>A XP_005246154.1:p.Val258Met
XM_005246097.3:c.772G>A XP_005246154.1:p.Val258Met
XM_005246098.2:c.772G>A XP_005246155.1:p.Val258Met
XM_005246098.3:c.772G>A XP_005246155.1:p.Val258Met
XM_011511503.1:c.772G>A XP_011509805.1:p.Val258Met
XM_017004516.2:c.772G>A XP_016860005.1:p.Val258Met