Canonical Allele Identifier: CA449650122
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431708C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463931C>T , CM000668.2:g.31463931C>T GRCh38
NC_000006.11:g.31431708C>T , CM000668.1:g.31431708C>T GRCh37
NC_000006.10:g.31539687C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.661C>T
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