Canonical Allele Identifier: CA449649646

Gene: HCP5

Linked Data

• gnomAD v4: 6-31463771-A-G
• MyVariant Identifiers: chr6:g.31431548A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463771A>G , CM000668.2:g.31463771A>G	GRCh38
NC_000006.11:g.31431548A>G , CM000668.1:g.31431548A>G	GRCh37
NC_000006.10:g.31539527A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.501A>G