Canonical Allele Identifier: CA1328655605
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216607G= , CM000664.2:g.218216607G= GRCh38
NC_000002.11:g.219081330G= , CM000664.1:g.219081330G= GRCh37
NC_000002.10:g.218789575G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_241416.2:n.338C=
XR_923908.1:n.335C=