Canonical Allele Identifier: CA449651002
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1441100044
gnomAD v3: 6-31464158-C-A
gnomAD v4: 6-31464158-C-A
MyVariant Identifiers: chr6:g.31431935C>A (hg19) chr6:g.31464158C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464158C>A , CM000668.2:g.31464158C>A GRCh38
NC_000006.11:g.31431935C>A , CM000668.1:g.31431935C>A GRCh37
NC_000006.10:g.31539914C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.888C>A
Search 100 bp 5'
Search 100 bp 3'