Canonical Allele Identifier: CA136868361
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs947248383
MyVariant Identifiers: chr6:g.31431303G>C (hg19) chr6:g.31463526G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463526G>C , CM000668.2:g.31463526G>C GRCh38
NC_000006.11:g.31431303G>C , CM000668.1:g.31431303G>C GRCh37
NC_000006.10:g.31539282G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.256G>C
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