Canonical Allele Identifier: CA2122788295
Community Standard Title: NC_000014.9:g.22013585A=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22013585A= , CM000676.2:g.22013585A= GRCh38
NC_000014.8:g.22481824A= , CM000676.1:g.22481824A= GRCh37
NC_000014.7:g.21551664A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000553572.2:n.1676A=