Canonical Allele Identifier: CA449652205
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1468827848
MyVariant Identifiers: chr6:g.31432174A>G (hg19) chr6:g.31464397A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464397A>G , CM000668.2:g.31464397A>G GRCh38
NC_000006.11:g.31432174A>G , CM000668.1:g.31432174A>G GRCh37
NC_000006.10:g.31540153A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1127A>G
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