Canonical Allele Identifier: CA449648496
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs2113961855
gnomAD v3: 6-31463525-T-C
gnomAD v4: 6-31463525-T-C
MyVariant Identifiers: chr6:g.31431302T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463525T>C , CM000668.2:g.31463525T>C GRCh38
NC_000006.11:g.31431302T>C , CM000668.1:g.31431302T>C GRCh37
NC_000006.10:g.31539281T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.255T>C