Canonical Allele Identifier: CA449648174
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1425949372
gnomAD v4: 6-31463417-A-G
MyVariant Identifiers: chr6:g.31431194A>G (hg19) chr6:g.31463417A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463417A>G , CM000668.2:g.31463417A>G GRCh38
NC_000006.11:g.31431194A>G , CM000668.1:g.31431194A>G GRCh37
NC_000006.10:g.31539173A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.147A>G
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