Canonical Allele Identifier: CA2626329379
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612352T>C , CM000676.2:g.94612352T>C GRCh38
NC_000014.8:g.95078689T>C , CM000676.1:g.95078689T>C GRCh37
NC_000014.7:g.94148442T>C NCBI36
NG_012879.1:g.4976T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000553947.1:c.860T>C