Canonical Allele Identifier: CA3712421
Gene: HCP5 HGNC NCBI
COSMIC:
COSM4003933 (not active)
MyVariant.info:
GRCh38 chr6:g.31463914G>T
GRCh37 chr6:g.31431691G>T
gnomAD v2:
6:31431691 G / T
gnomAD v3:
6:31463914 G / T
gnomAD v4:
chr6-31463914-G-T
Joint Max Group AF 0.1543054 (AFR)
Genomes Max Group AF 0.15491381 (AFR)
Exomes Max Group AF 0.14702014 (AFR)
dbSNP:
2255221
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463914G>T , CM000668.2:g.31463914G>T GRCh38
NC_000006.11:g.31431691G>T , CM000668.1:g.31431691G>T GRCh37
NC_000006.10:g.31539670G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.644G>T
Search 100 bp 5'
Search 100 bp 3'