Canonical Allele Identifier: CA290788946
Gene: CCR10 HGNC NCBI
CNTNAP1 HGNC NCBI

Linked Data

dbSNP Id: rs966134103
gnomAD v3: 17-42682526-T-C
gnomAD v4: 17-42682526-T-C
MyVariant Identifiers: chr17:g.40834544T>C (hg19) chr17:g.42682526T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682526T>C , CM000679.2:g.42682526T>C GRCh38
NC_000017.10:g.40834544T>C , CM000679.1:g.40834544T>C GRCh37
NC_000017.9:g.38088070T>C NCBI36
NG_042091.1:g.4913T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000591568.1:c.-643+1290A>G (CCR10) ENSP00000467331.1:n.-643+1290A>G
ENST00000591765.1:c.-848A>G (CCR10) ENSP00000468135.1:n.-848A>G
XM_017025238.1:c.-304T>C (CNTNAP1) XP_016880727.1:n.-304T>C
XM_024451011.1:c.-304T>C (CNTNAP1) XP_024306779.1:n.-304T>C
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