Canonical Allele Identifier: CA449652300

Gene: HCP5

Linked Data

• dbSNP Id: rs1485047875
• gnomAD v2: 6-31432191-C-T
• gnomAD v3: 6-31464414-C-T
• gnomAD v4: 6-31464414-C-T
• MyVariant Identifiers: chr6:g.31432191C>T (hg19) ; chr6:g.31464414C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464414C>T , CM000668.2:g.31464414C>T	GRCh38
NC_000006.11:g.31432191C>T , CM000668.1:g.31432191C>T	GRCh37
NC_000006.10:g.31540170C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1144C>T