Canonical Allele Identifier: CA2626329372
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612344A>T , CM000676.2:g.94612344A>T GRCh38
NC_000014.8:g.95078681A>T , CM000676.1:g.95078681A>T GRCh37
NC_000014.7:g.94148434A>T NCBI36
NG_012879.1:g.4968A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000553947.1:c.852A>T