Canonical Allele Identifier: CA449650475

Gene: HCP5

Linked Data

• dbSNP Id: rs1295051354
• gnomAD v2: 6-31431830-G-T
• gnomAD v3: 6-31464053-G-T
• gnomAD v4: 6-31464053-G-T
• MyVariant Identifiers: chr6:g.31431830G>T (hg19) ; chr6:g.31464053G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464053G>T , CM000668.2:g.31464053G>T	GRCh38
NC_000006.11:g.31431830G>T , CM000668.1:g.31431830G>T	GRCh37
NC_000006.10:g.31539809G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.783G>T