Canonical Allele Identifier: CA622672265
Gene: CCL17 HGNC NCBI

Linked Data

dbSNP Id: rs1214848118
gnomAD v2: 16-57447453-C-T
gnomAD v3: 16-57413541-C-T
gnomAD v4: 16-57413541-C-T
MyVariant Identifiers: chr16:g.57447453C>T (hg19) chr16:g.57413541C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57413541C>T , CM000678.2:g.57413541C>T GRCh38
NC_000016.9:g.57447453C>T , CM000678.1:g.57447453C>T GRCh37
NC_000016.8:g.56004954C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219244.9:c.-59-333C>T MANE Select ENSP00000219244.4:n.-59-333C>T
ENST00000219244.8:c.-59-333C>T ENSP00000219244.4:n.-59-333C>T
NM_002987.2:c.-59-333C>T NP_002978.1:n.-59-333C>T
XM_011523256.1:c.26-333C>T XP_011521558.1:n.26-333C>T
XM_011523256.2:c.26-333C>T XP_011521558.1:n.26-333C>T
XM_017023530.1:c.26-330C>T XP_016879019.1:n.26-330C>T
NM_002987.3:c.-59-333C>T MANE Select NP_002978.1:n.-59-333C>T
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