Canonical Allele Identifier: CA449652188
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31432171C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464394C>A , CM000668.2:g.31464394C>A GRCh38
NC_000006.11:g.31432171C>A , CM000668.1:g.31432171C>A GRCh37
NC_000006.10:g.31540150C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1124C>A
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