Canonical Allele Identifier: CA3712441
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs2243621
ExAC: 6:31431820 C / T
gnomAD v2: 6-31431820-C-T
gnomAD v3: 6-31464043-C-T
gnomAD v4: 6-31464043-C-T
MyVariant Identifiers: chr6:g.31431820C>T (hg19) chr6:g.31464043C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464043C>T , CM000668.2:g.31464043C>T GRCh38
NC_000006.11:g.31431820C>T , CM000668.1:g.31431820C>T GRCh37
NC_000006.10:g.31539799C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.773C>T
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