Canonical Allele Identifier: CA136868381
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs900652852
gnomAD v3: 6-31463577-C-T
gnomAD v4: 6-31463577-C-T
MyVariant Identifiers: chr6:g.31431354C>T (hg19) chr6:g.31463577C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463577C>T , CM000668.2:g.31463577C>T GRCh38
NC_000006.11:g.31431354C>T , CM000668.1:g.31431354C>T GRCh37
NC_000006.10:g.31539333C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.307C>T
Search 100 bp 5'
Search 100 bp 3'