Canonical Allele Identifier: CA136868624
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1003992193
MyVariant Identifiers: chr6:g.31431707A>T (hg19) chr6:g.31463930A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463930A>T , CM000668.2:g.31463930A>T GRCh38
NC_000006.11:g.31431707A>T , CM000668.1:g.31431707A>T GRCh37
NC_000006.10:g.31539686A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.660A>T
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