Canonical Allele Identifier: CA2156070621
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612252C= , CM000676.2:g.94612252C= GRCh38
NC_000014.8:g.95078589C= , CM000676.1:g.95078589C= GRCh37
NC_000014.7:g.94148342C= NCBI36
NG_012879.1:g.4876C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553947.1:c.805-45C=