Canonical Allele Identifier: CA1595159013
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580674T= , CM000667.2:g.159580674T= GRCh38
NC_000005.9:g.159007682T= , CM000667.1:g.159007682T= GRCh37
NC_000005.8:g.158940260T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+239T=
XR_941140.1:n.2075+239T=
XR_941141.1:n.570+239T=
XR_941139.2:n.2229+239T=