Canonical Allele Identifier: CA449650343

Gene: HCP5

Linked Data

• gnomAD v4: 6-31464011-G-T
• MyVariant Identifiers: chr6:g.31431788G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464011G>T , CM000668.2:g.31464011G>T	GRCh38
NC_000006.11:g.31431788G>T , CM000668.1:g.31431788G>T	GRCh37
NC_000006.10:g.31539767G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040662.1:n.741G>T