Canonical Allele Identifier: CA281564788
Gene: CCL17 HGNC NCBI

Linked Data

dbSNP Id: rs910211490
MyVariant Identifiers: chr16:g.57413443C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57413443C>G , CM000678.2:g.57413443C>G GRCh38
NC_000016.9:g.57447355C>G , CM000678.1:g.57447355C>G GRCh37
NC_000016.8:g.56004856C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219244.9:c.-59-431C>G MANE Select ENSP00000219244.4:n.-59-431C>G
ENST00000219244.8:c.-59-431C>G ENSP00000219244.4:n.-59-431C>G
NM_002987.2:c.-59-431C>G NP_002978.1:n.-59-431C>G
XM_011523256.1:c.26-431C>G XP_011521558.1:n.26-431C>G
XM_011523256.2:c.26-431C>G XP_011521558.1:n.26-431C>G
XM_017023530.1:c.26-428C>G XP_016879019.1:n.26-428C>G
NM_002987.3:c.-59-431C>G MANE Select NP_002978.1:n.-59-431C>G
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