Canonical Allele Identifier: CA1149683779
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2567432G= , CM000663.2:g.2567432G= GRCh38
NC_000001.10:g.2498871G= , CM000663.1:g.2498871G= GRCh37
NC_000001.9:g.2475547C= NCBI36
NG_047096.1:g.16068G=

Transcript Alleles

HGVS Amino-acid Change
NR_121638.1:n.71+827G=