Canonical Allele Identifier: CA449650390
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1428807868
gnomAD v2: 6-31431804-T-C
gnomAD v3: 6-31464027-T-C
gnomAD v4: 6-31464027-T-C
MyVariant Identifiers: chr6:g.31431804T>C (hg19) chr6:g.31464027T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464027T>C , CM000668.2:g.31464027T>C GRCh38
NC_000006.11:g.31431804T>C , CM000668.1:g.31431804T>C GRCh37
NC_000006.10:g.31539783T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.757T>C
Search 100 bp 5'
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