Canonical Allele Identifier: CA485017782
Gene:

Linked Data

MyVariant Identifiers: chr13:g.113756606A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113102292A>T , CM000675.2:g.113102292A>T GRCh38
NC_000013.10:g.113756606A>T , CM000675.1:g.113756606A>T GRCh37
NC_000013.9:g.112804607A>T NCBI36
NG_009262.1:g.1502A>T , LRG_554:g.1502A>T