Canonical Allele Identifier: CA1261549148
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74711963T= , CM000664.2:g.74711963T= GRCh38
NC_000002.11:g.74939090T= , CM000664.1:g.74939090T= GRCh37
NC_000002.10:g.74792598T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427047.4:n.276T=