Canonical Allele Identifier: CA232382
Gene: CCL23 HGNC NCBI

Linked Data

ClinVar Variation Id: 92029
ClinVar RCV Id: RCV000122586
dbSNP Id: rs386352289
ExAC: 17:34340854 G / A
gnomAD v2: 17-34340854-G-A
gnomAD v3: 17-36013814-G-A
gnomAD v4: 17-36013814-G-A
MyVariant Identifiers: chr17:g.34340854G>A (hg19) chr17:g.36013814G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.36013814G>A , CM000679.2:g.36013814G>A GRCh38
NC_000017.10:g.34340854G>A , CM000679.1:g.34340854G>A GRCh37
NC_000017.9:g.31364967G>A NCBI36
NG_029876.2:g.9155C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000615050.2:c.232C>T MANE Select ENSP00000481357.1:p.Arg78Ter
ENST00000612516.4:c.181C>T ENSP00000484748.1:p.Arg61Ter
ENST00000615050.1:c.232C>T ENSP00000481357.1:p.Arg78Ter
NM_005064.5:c.232C>T NP_005055.3:p.Arg78Ter
NM_145898.3:c.181C>T NP_665905.2:p.Arg61Ter
XR_429910.2:n.310C>T
XR_001752854.1:n.211+3672G>A
XR_429910.3:n.514C>T
NM_005064.6:c.232C>T MANE Select NP_005055.3:p.Arg78Ter
NM_145898.4:c.181C>T NP_665905.2:p.Arg61Ter
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