Canonical Allele Identifier: CA1619157032
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439683C= , CM000668.2:g.31439683C= GRCh38
NC_000006.11:g.31407460C= , CM000668.1:g.31407460C= GRCh37
NC_000006.10:g.31515439C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.424G=