Canonical Allele Identifier: CA2156070620
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612248A= , CM000676.2:g.94612248A= GRCh38
NC_000014.8:g.95078585A= , CM000676.1:g.95078585A= GRCh37
NC_000014.7:g.94148338A= NCBI36
NG_012879.1:g.4872A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553947.1:c.805-49A=