Canonical Allele Identifier: CA136868460
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs868800508
MyVariant Identifiers: chr6:g.31431497G>A (hg19) chr6:g.31463720G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463720G>A , CM000668.2:g.31463720G>A GRCh38
NC_000006.11:g.31431497G>A , CM000668.1:g.31431497G>A GRCh37
NC_000006.10:g.31539476G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.450G>A
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