Canonical Allele Identifier: CA136868318
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs992215987
gnomAD v3: 6-31463392-G-A
gnomAD v4: 6-31463392-G-A
MyVariant Identifiers: chr6:g.31431169G>A (hg19) chr6:g.31463392G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463392G>A , CM000668.2:g.31463392G>A GRCh38
NC_000006.11:g.31431169G>A , CM000668.1:g.31431169G>A GRCh37
NC_000006.10:g.31539148G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.122G>A
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