Canonical Allele Identifier: CA281564772
Gene: CCL17 HGNC NCBI

Linked Data

dbSNP Id: rs987571167
gnomAD v3: 16-57413423-G-A
gnomAD v4: 16-57413423-G-A
MyVariant Identifiers: chr16:g.57447335G>A (hg19) chr16:g.57413423G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57413423G>A , CM000678.2:g.57413423G>A GRCh38
NC_000016.9:g.57447335G>A , CM000678.1:g.57447335G>A GRCh37
NC_000016.8:g.56004836G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219244.9:c.-59-451G>A MANE Select ENSP00000219244.4:n.-59-451G>A
ENST00000219244.8:c.-59-451G>A ENSP00000219244.4:n.-59-451G>A
NM_002987.2:c.-59-451G>A NP_002978.1:n.-59-451G>A
XM_011523256.1:c.26-451G>A XP_011521558.1:n.26-451G>A
XM_011523256.2:c.26-451G>A XP_011521558.1:n.26-451G>A
XM_017023530.1:c.26-448G>A XP_016879019.1:n.26-448G>A
NM_002987.3:c.-59-451G>A MANE Select NP_002978.1:n.-59-451G>A
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