Canonical Allele Identifier: CA2488842759
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11117441C= , CM000664.2:g.11117441C= GRCh38
NC_000002.11:g.11257567C= , CM000664.1:g.11257567C= GRCh37
NC_000002.10:g.11175018C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040080.1:n.984+3322G=