Canonical Allele Identifier: CA449652304
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31432191C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464414C>G , CM000668.2:g.31464414C>G GRCh38
NC_000006.11:g.31432191C>G , CM000668.1:g.31432191C>G GRCh37
NC_000006.10:g.31540170C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1144C>G
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