Canonical Allele Identifier: CA449648369

Gene: HCP5

Linked Data

• dbSNP Id: rs1283581403
• gnomAD v2: 6-31431260-T-G
• gnomAD v3: 6-31463483-T-G
• gnomAD v4: 6-31463483-T-G
• MyVariant Identifiers: chr6:g.31431260T>G (hg19) ; chr6:g.31463483T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463483T>G , CM000668.2:g.31463483T>G	GRCh38
NC_000006.11:g.31431260T>G , CM000668.1:g.31431260T>G	GRCh37
NC_000006.10:g.31539239T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.213T>G