Canonical Allele Identifier: CA1261549150
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74711969T= , CM000664.2:g.74711969T= GRCh38
NC_000002.11:g.74939096T= , CM000664.1:g.74939096T= GRCh37
NC_000002.10:g.74792604T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427047.4:n.282T=