Canonical Allele Identifier: CA449649766

Gene: HCP5

Linked Data

• gnomAD v4: 6-31463805-T-C
• MyVariant Identifiers: chr6:g.31431582T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463805T>C , CM000668.2:g.31463805T>C	GRCh38
NC_000006.11:g.31431582T>C , CM000668.1:g.31431582T>C	GRCh37
NC_000006.10:g.31539561T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040662.1:n.535T>C