Canonical Allele Identifier: CA449648442

Gene: HCP5

Linked Data

• dbSNP Id: rs1452412222
• gnomAD v2: 6-31431284-A-C
• gnomAD v3: 6-31463507-A-C
• gnomAD v4: 6-31463507-A-C
• MyVariant Identifiers: chr6:g.31431284A>C (hg19) ; chr6:g.31463507A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463507A>C , CM000668.2:g.31463507A>C	GRCh38
NC_000006.11:g.31431284A>C , CM000668.1:g.31431284A>C	GRCh37
NC_000006.10:g.31539263A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.237A>C