Canonical Allele Identifier: CA101676572
Gene:

Linked Data

dbSNP Id: rs908124573
MyVariant Identifiers: chr4:g.99353053C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99353053C>T , CM000666.2:g.99353053C>T GRCh38
NC_000004.11:g.100274210C>T , CM000666.1:g.100274210C>T GRCh37
NC_000004.10:g.100493233C>T NCBI36
NG_011718.1:g.4708G>A