Canonical Allele Identifier: CA1619157141
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439990C= , CM000668.2:g.31439990C= GRCh38
NC_000006.11:g.31407767C= , CM000668.1:g.31407767C= GRCh37
NC_000006.10:g.31515746C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.117G=