Canonical Allele Identifier: CA8075182
Gene: CCL22 HGNC NCBI

Linked Data

dbSNP Id: rs4359426
ExAC: 16:57392733 A / C
gnomAD v2: 16-57392733-A-C
gnomAD v3: 16-57358821-A-C
gnomAD v4: 16-57358821-A-C
MyVariant Identifiers: chr16:g.57392733A>C (hg19) chr16:g.57358821A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57358821A>C , CM000678.2:g.57358821A>C GRCh38
NC_000016.9:g.57392733A>C , CM000678.1:g.57392733A>C GRCh37
NC_000016.8:g.55950234A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000219235.5:c.5A>C MANE Select ENSP00000219235.4:p.Asp2Ala
ENST00000219235.4:c.5A>C ENSP00000219235.4:p.Asp2Ala
NM_002990.4:c.5A>C NP_002981.2:p.Asp2Ala
NM_002990.5:c.5A>C MANE Select NP_002981.2:p.Asp2Ala
Search 100 bp 5'
Search 100 bp 3'