Canonical Allele Identifier: CA449649782
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31463810-C-T
MyVariant Identifiers: chr6:g.31431587C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463810C>T , CM000668.2:g.31463810C>T GRCh38
NC_000006.11:g.31431587C>T , CM000668.1:g.31431587C>T GRCh37
NC_000006.10:g.31539566C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.540C>T
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