Canonical Allele Identifier: CA449650344
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1762861762
gnomAD v4: 6-31464011-G-A
MyVariant Identifiers: chr6:g.31431788G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464011G>A , CM000668.2:g.31464011G>A GRCh38
NC_000006.11:g.31431788G>A , CM000668.1:g.31431788G>A GRCh37
NC_000006.10:g.31539767G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.741G>A