Canonical Allele Identifier: CA3712399
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs17206855
ExAC: 6:31431539 T / C
gnomAD v2: 6-31431539-T-C
gnomAD v3: 6-31463762-T-C
gnomAD v4: 6-31463762-T-C
COSMIC: COSM1666267
MyVariant Identifiers: chr6:g.31431539T>C (hg19) chr6:g.31463762T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463762T>C , CM000668.2:g.31463762T>C GRCh38
NC_000006.11:g.31431539T>C , CM000668.1:g.31431539T>C GRCh37
NC_000006.10:g.31539518T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.492T>C
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