Canonical Allele Identifier: CA1653130392
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805157C= , CM000668.2:g.105805157C= GRCh38
NC_000006.11:g.106253032C= , CM000668.1:g.106253032C= GRCh37
NC_000006.10:g.106359725C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24900G=
XR_001744274.1:n.438+24900G=
XR_001744275.1:n.337+24900G=