Canonical Allele Identifier: CA449652191
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1176599702
gnomAD v3: 6-31464394-C-T
gnomAD v4: 6-31464394-C-T
MyVariant Identifiers: chr6:g.31432171C>T (hg19) chr6:g.31464394C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464394C>T , CM000668.2:g.31464394C>T GRCh38
NC_000006.11:g.31432171C>T , CM000668.1:g.31432171C>T GRCh37
NC_000006.10:g.31540150C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1124C>T
Search 100 bp 5'
Search 100 bp 3'