Canonical Allele Identifier: CA449649786
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31463811-T-C
MyVariant Identifiers: chr6:g.31431588T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463811T>C , CM000668.2:g.31463811T>C GRCh38
NC_000006.11:g.31431588T>C , CM000668.1:g.31431588T>C GRCh37
NC_000006.10:g.31539567T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.541T>C
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