Canonical Allele Identifier: CA3712443
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs778370607
ExAC: 6:31431824 T / C
gnomAD v2: 6-31431824-T-C
gnomAD v4: 6-31464047-T-C
MyVariant Identifiers: chr6:g.31431824T>C (hg19) chr6:g.31464047T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464047T>C , CM000668.2:g.31464047T>C GRCh38
NC_000006.11:g.31431824T>C , CM000668.1:g.31431824T>C GRCh37
NC_000006.10:g.31539803T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.777T>C
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