Canonical Allele Identifier: CA2129379088
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384952T= , CM000676.2:g.36384952T= GRCh38
NC_000014.8:g.36854157T= , CM000676.1:g.36854157T= GRCh37
NC_000014.7:g.35923908T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12207T= XP_011535730.1:n.319-12207T=
XR_943756.1:n.358+23856T=