Canonical Allele Identifier: CA3712415
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs192776040
ExAC: 6:31431643 C / T
gnomAD v2: 6-31431643-C-T
gnomAD v3: 6-31463866-C-T
gnomAD v4: 6-31463866-C-T
MyVariant Identifiers: chr6:g.31431643C>T (hg19) chr6:g.31463866C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463866C>T , CM000668.2:g.31463866C>T GRCh38
NC_000006.11:g.31431643C>T , CM000668.1:g.31431643C>T GRCh37
NC_000006.10:g.31539622C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.596C>T
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