Canonical Allele Identifier: CA449649826
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31463825-G-T
MyVariant Identifiers: chr6:g.31431602G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463825G>T , CM000668.2:g.31463825G>T GRCh38
NC_000006.11:g.31431602G>T , CM000668.1:g.31431602G>T GRCh37
NC_000006.10:g.31539581G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.555G>T