Canonical Allele Identifier: CA1648334832
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.95519463C= , CM000668.2:g.95519463C= GRCh38
NC_000006.11:g.95967339C= , CM000668.1:g.95967339C= GRCh37
NC_000006.10:g.96074060C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942795.1:n.103G=