Canonical Allele Identifier: CA3712433

Gene: HCP5

Linked Data

• dbSNP Id: rs759650489
• ExAC: 6:31431758 C / T
• gnomAD v2: 6-31431758-C-T
• gnomAD v4: 6-31463981-C-T
• MyVariant Identifiers: chr6:g.31431758C>T (hg19) ; chr6:g.31463981C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463981C>T , CM000668.2:g.31463981C>T	GRCh38
NC_000006.11:g.31431758C>T , CM000668.1:g.31431758C>T	GRCh37
NC_000006.10:g.31539737C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.711C>T