Canonical Allele Identifier: CA290788958
Gene: CCR10 HGNC NCBI
CNTNAP1 HGNC NCBI

Linked Data

dbSNP Id: rs768345891
MyVariant Identifiers: chr17:g.40834545C>G (hg19) chr17:g.42682527C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682527C>G , CM000679.2:g.42682527C>G GRCh38
NC_000017.10:g.40834545C>G , CM000679.1:g.40834545C>G GRCh37
NC_000017.9:g.38088071C>G NCBI36
NG_042091.1:g.4914C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000591568.1:c.-643+1289G>C (CCR10) ENSP00000467331.1:n.-643+1289G>C
ENST00000591765.1:c.-849G>C (CCR10) ENSP00000468135.1:n.-849G>C
XM_017025238.1:c.-303C>G (CNTNAP1) XP_016880727.1:n.-303C>G
XM_024451011.1:c.-303C>G (CNTNAP1) XP_024306779.1:n.-303C>G
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