Canonical Allele Identifier: CA136868327
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs182110306
gnomAD v4: 6-31463397-G-T
MyVariant Identifiers: chr6:g.31431174G>T (hg19) chr6:g.31463397G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463397G>T , CM000668.2:g.31463397G>T GRCh38
NC_000006.11:g.31431174G>T , CM000668.1:g.31431174G>T GRCh37
NC_000006.10:g.31539153G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.127G>T
Search 100 bp 5'
Search 100 bp 3'