Canonical Allele Identifier: CA2156070662
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612343G= , CM000676.2:g.94612343G= GRCh38
NC_000014.8:g.95078680G= , CM000676.1:g.95078680G= GRCh37
NC_000014.7:g.94148433G= NCBI36
NG_012879.1:g.4967G=

Transcript Alleles

HGVS Amino-acid change
ENST00000553947.1:c.851G=