Canonical Allele Identifier: CA2493232064
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20485639T= , CM000664.2:g.20485639T= GRCh38
NC_000002.11:g.20685400T= , CM000664.1:g.20685400T= GRCh37
NC_000002.10:g.20548881T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_157978.1:n.530+3099A=