Canonical Allele Identifier: CA1328655598
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216591C= , CM000664.2:g.218216591C= GRCh38
NC_000002.11:g.219081314C= , CM000664.1:g.219081314C= GRCh37
NC_000002.10:g.218789559C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241416.2:n.354G=
XR_923908.1:n.351G=