Canonical Allele Identifier: CA449649551

Gene: HCP5

Linked Data

• dbSNP Id: rs1762845225
• gnomAD v4: 6-31463757-G-A
• MyVariant Identifiers: chr6:g.31431534G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463757G>A , CM000668.2:g.31463757G>A	GRCh38
NC_000006.11:g.31431534G>A , CM000668.1:g.31431534G>A	GRCh37
NC_000006.10:g.31539513G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.487G>A