Canonical Allele Identifier: CA2493232093
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20485711G= , CM000664.2:g.20485711G= GRCh38
NC_000002.11:g.20685472G= , CM000664.1:g.20685472G= GRCh37
NC_000002.10:g.20548953G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_157978.1:n.530+3027C=