Canonical Allele Identifier: CA281558248
Gene: CCL22 HGNC NCBI

Linked Data

dbSNP Id: rs4359426
gnomAD v4: 16-57358821-A-T
MyVariant Identifiers: chr16:g.57392733A>T (hg19) chr16:g.57358821A>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000219235.5:c.5A>T MANE Select ENSP00000219235.4:p.Asp2Val
ENST00000219235.4:c.5A>T ENSP00000219235.4:p.Asp2Val
NM_002990.4:c.5A>T NP_002981.2:p.Asp2Val
NM_002990.5:c.5A>T MANE Select NP_002981.2:p.Asp2Val
Search 100 bp 5'
Search 100 bp 3'