Canonical Allele Identifier: CA1468682087
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74554016A= , CM000666.2:g.74554016A= GRCh38
NC_000004.11:g.75419733A= , CM000666.1:g.75419733A= GRCh37
NC_000004.10:g.75638597A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741513.1:n.167-1184T=