Canonical Allele Identifier: CA449648127
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1168926392
MyVariant Identifiers: chr6:g.31431179C>G (hg19) chr6:g.31463402C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463402C>G , CM000668.2:g.31463402C>G GRCh38
NC_000006.11:g.31431179C>G , CM000668.1:g.31431179C>G GRCh37
NC_000006.10:g.31539158C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.132C>G
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