Canonical Allele Identifier: CA2156070670
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612354T= , CM000676.2:g.94612354T= GRCh38
NC_000014.8:g.95078691T= , CM000676.1:g.95078691T= GRCh37
NC_000014.7:g.94148444T= NCBI36
NG_012879.1:g.4978T=

Transcript Alleles

HGVS Amino-acid change
ENST00000553947.1:c.862T=