Canonical Allele Identifier: CA2626329378
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612351C>T , CM000676.2:g.94612351C>T GRCh38
NC_000014.8:g.95078688C>T , CM000676.1:g.95078688C>T GRCh37
NC_000014.7:g.94148441C>T NCBI36
NG_012879.1:g.4975C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553947.1:c.859C>T