Canonical Allele Identifier: CA449648169

Gene: HCP5

Linked Data

• gnomAD v4: 6-31463415-C-T
• MyVariant Identifiers: chr6:g.31431192C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463415C>T , CM000668.2:g.31463415C>T	GRCh38
NC_000006.11:g.31431192C>T , CM000668.1:g.31431192C>T	GRCh37
NC_000006.10:g.31539171C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.145C>T