Canonical Allele Identifier: CA1889304372
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8659167T= , CM000672.2:g.8659167T= GRCh38
NC_000010.10:g.8701130T= , CM000672.1:g.8701130T= GRCh37
NC_000010.9:g.8741136T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.181A=
XR_001747277.1:n.150A=