Canonical Allele Identifier: CA449650125
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1360973986
gnomAD v2: 6-31431709-C-T
MyVariant Identifiers: chr6:g.31431709C>T (hg19) chr6:g.31463932C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463932C>T , CM000668.2:g.31463932C>T GRCh38
NC_000006.11:g.31431709C>T , CM000668.1:g.31431709C>T GRCh37
NC_000006.10:g.31539688C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.662C>T
Search 100 bp 5'
Search 100 bp 3'