Canonical Allele Identifier: CA449650222
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1762859491
gnomAD v3: 6-31463967-C-T
gnomAD v4: 6-31463967-C-T
MyVariant Identifiers: chr6:g.31431744C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463967C>T , CM000668.2:g.31463967C>T GRCh38
NC_000006.11:g.31431744C>T , CM000668.1:g.31431744C>T GRCh37
NC_000006.10:g.31539723C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.697C>T
Search 100 bp 5'
Search 100 bp 3'