Canonical Allele Identifier: CA444225181
Gene:

Linked Data

MyVariant Identifiers: chr5:g.56195914T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56900087T>G , CM000667.2:g.56900087T>G GRCh38
NC_000005.9:g.56195914T>G , CM000667.1:g.56195914T>G GRCh37
NC_000005.8:g.56231671T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948346.1:n.83-1791A>C
XR_948347.3:n.316A>C