Canonical Allele Identifier: CA105563444
Gene:

Linked Data

dbSNP Id: rs189003721
MyVariant Identifiers: chr4:g.126075128A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.126075128A>T , CM000666.2:g.126075128A>T GRCh38
NC_000004.11:g.126996283A>T , CM000666.1:g.126996283A>T GRCh37
NC_000004.10:g.127215733A>T NCBI36