Canonical Allele Identifier: CA449650108

Gene: HCP5

Linked Data

• dbSNP Id: rs1433173839
• gnomAD v2: 6-31431703-T-C
• gnomAD v4: 6-31463926-T-C
• MyVariant Identifiers: chr6:g.31431703T>C (hg19) ; chr6:g.31463926T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463926T>C , CM000668.2:g.31463926T>C	GRCh38
NC_000006.11:g.31431703T>C , CM000668.1:g.31431703T>C	GRCh37
NC_000006.10:g.31539682T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.656T>C