Canonical Allele Identifier: CA2626329376
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612349T>G , CM000676.2:g.94612349T>G GRCh38
NC_000014.8:g.95078686T>G , CM000676.1:g.95078686T>G GRCh37
NC_000014.7:g.94148439T>G NCBI36
NG_012879.1:g.4973T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553947.1:c.857T>G