Canonical Allele Identifier: CA1439212635
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578016C= , CM000666.2:g.12578016C= GRCh38
NC_000004.11:g.12579640C= , CM000666.1:g.12579640C= GRCh37
NC_000004.10:g.12188738C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31326G=
XR_001741374.1:n.254+44639G=
XR_925406.3:n.140+31326G=