Canonical Allele Identifier: CA2156070626
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612265A= , CM000676.2:g.94612265A= GRCh38
NC_000014.8:g.95078602A= , CM000676.1:g.95078602A= GRCh37
NC_000014.7:g.94148355A= NCBI36
NG_012879.1:g.4889A=

Transcript Alleles

HGVS Amino-acid change
ENST00000553947.1:c.805-32A=