Canonical Allele Identifier: CA136868838
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1022256405
gnomAD v2: 6-31432212-T-C
gnomAD v3: 6-31464435-T-C
gnomAD v4: 6-31464435-T-C
MyVariant Identifiers: chr6:g.31432212T>C (hg19) chr6:g.31464435T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464435T>C , CM000668.2:g.31464435T>C GRCh38
NC_000006.11:g.31432212T>C , CM000668.1:g.31432212T>C GRCh37
NC_000006.10:g.31540191T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1165T>C
Search 100 bp 5'
Search 100 bp 3'