Canonical Allele Identifier: CA100778601
Gene:

Linked Data

dbSNP Id: rs966764141
MyVariant Identifiers: chr4:g.87155047G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87155047G>C , CM000666.2:g.87155047G>C GRCh38
NC_000004.11:g.88076199G>C , CM000666.1:g.88076199G>C GRCh37
NC_000004.10:g.88295223G>C NCBI36