Canonical Allele Identifier: CA722066805
Gene: CCL17 HGNC NCBI

Linked Data

dbSNP Id: rs223828
MyVariant Identifiers: chr16:g.57447414T>A (hg19) chr16:g.57413502T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57413502T>A , CM000678.2:g.57413502T>A GRCh38
NC_000016.9:g.57447414T>A , CM000678.1:g.57447414T>A GRCh37
NC_000016.8:g.56004915T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000219244.9:c.-59-372T>A MANE Select ENSP00000219244.4:n.-59-372T>A
ENST00000219244.8:c.-59-372T>A ENSP00000219244.4:n.-59-372T>A
NM_002987.2:c.-59-372T>A NP_002978.1:n.-59-372T>A
XM_011523256.1:c.26-372T>A XP_011521558.1:n.26-372T>A
XM_011523256.2:c.26-372T>A XP_011521558.1:n.26-372T>A
XM_017023530.1:c.26-369T>A XP_016879019.1:n.26-369T>A
NM_002987.3:c.-59-372T>A MANE Select NP_002978.1:n.-59-372T>A
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