Canonical Allele Identifier: CA449648585
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431333C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463556C>A , CM000668.2:g.31463556C>A GRCh38
NC_000006.11:g.31431333C>A , CM000668.1:g.31431333C>A GRCh37
NC_000006.10:g.31539312C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.286C>A
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