Canonical Allele Identifier: CA117655313
Gene:

Linked Data

dbSNP Id: rs1005481698
MyVariant Identifiers: chr5:g.39978759T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.39978759T>C , CM000667.2:g.39978759T>C GRCh38
NC_000005.9:g.39978861T>C , CM000667.1:g.39978861T>C GRCh37
NC_000005.8:g.40014618T>C NCBI36