Canonical Allele Identifier: CA2626329381
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612354T>C , CM000676.2:g.94612354T>C GRCh38
NC_000014.8:g.95078691T>C , CM000676.1:g.95078691T>C GRCh37
NC_000014.7:g.94148444T>C NCBI36
NG_012879.1:g.4978T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000553947.1:c.862T>C