Canonical Allele Identifier: CA2561660936
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612341G>C , CM000676.2:g.94612341G>C GRCh38
NC_000014.8:g.95078678G>C , CM000676.1:g.95078678G>C GRCh37
NC_000014.7:g.94148431G>C NCBI36
NG_012879.1:g.4965G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000553947.1:c.849G>C