Canonical Allele Identifier: CA2156070622
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612259G= , CM000676.2:g.94612259G= GRCh38
NC_000014.8:g.95078596G= , CM000676.1:g.95078596G= GRCh37
NC_000014.7:g.94148349G= NCBI36
NG_012879.1:g.4883G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553947.1:c.805-38G=