Canonical Allele Identifier: CA449652155

Gene: HCP5

Linked Data

• gnomAD v4: 6-31464388-G-C
• MyVariant Identifiers: chr6:g.31432165G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464388G>C , CM000668.2:g.31464388G>C	GRCh38
NC_000006.11:g.31432165G>C , CM000668.1:g.31432165G>C	GRCh37
NC_000006.10:g.31540144G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1118G>C