Canonical Allele Identifier: CA2750840837
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016096A>G , CM000664.2:g.88016096A>G GRCh38
NC_000002.11:g.88315615A>G , CM000664.1:g.88315615A>G GRCh37
NC_000002.10:g.88096730A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.441A>G
XR_940336.3:n.441A>G