Canonical Allele Identifier: CA1905919974
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318547C= , CM000672.2:g.43318547C= GRCh38
NC_000010.10:g.43813995C= , CM000672.1:g.43813995C= GRCh37
NC_000010.9:g.43134001C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.60C=
XR_945902.2:n.150C=