Canonical Allele Identifier: CA823893763

Gene: HCP5

Linked Data

• dbSNP Id: rs1329492837
• gnomAD v4: 6-31464017-TGTAGTTCAATGG-T
• MyVariant Identifiers: chr6:g.31431795_31431806del (hg19) ; chr6:g.31464018_31464029del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464019_31464030del , CM000668.2:g.31464019_31464030del	GRCh38
NC_000006.11:g.31431796_31431807del , CM000668.1:g.31431796_31431807del	GRCh37
NC_000006.10:g.31539775_31539786del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040662.1:n.749_760del