Canonical Allele Identifier: CA449650690
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431886G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464109G>T , CM000668.2:g.31464109G>T GRCh38
NC_000006.11:g.31431886G>T , CM000668.1:g.31431886G>T GRCh37
NC_000006.10:g.31539865G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.839G>T
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