Canonical Allele Identifier: CA2224601255

Gene: CCL17

Linked Data

• dbSNP Id: rs1902815833

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.57413346C>T , CM000678.2:g.57413346C>T	GRCh38
NC_000016.9:g.57447258C>T , CM000678.1:g.57447258C>T	GRCh37
NC_000016.8:g.56004759C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219244.9:c.-59-528C>T MANE Select	ENSP00000219244.4:n.-59-528C>T
ENST00000219244.8:c.-59-528C>T	ENSP00000219244.4:n.-59-528C>T
NM_002987.2:c.-59-528C>T	NP_002978.1:n.-59-528C>T
XM_011523256.1:c.26-528C>T	XP_011521558.1:n.26-528C>T
XM_011523256.2:c.26-528C>T	XP_011521558.1:n.26-528C>T
XM_017023530.1:c.26-525C>T	XP_016879019.1:n.26-525C>T
NM_002987.3:c.-59-528C>T MANE Select	NP_002978.1:n.-59-528C>T