Canonical Allele Identifier: CA1595159558
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159581039C= , CM000667.2:g.159581039C= GRCh38
NC_000005.9:g.159008046C= , CM000667.1:g.159008046C= GRCh37
NC_000005.8:g.158940624C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941139.1:n.2075+604C=
XR_941140.1:n.2075+604C=
XR_941141.1:n.570+604C=
XR_941139.2:n.2229+604C=