Canonical Allele Identifier: CA2580739359
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46352969T>A , CM000669.2:g.46352969T>A GRCh38
NC_000007.13:g.46392567T>A , CM000669.1:g.46392567T>A GRCh37
NC_000007.12:g.46359092T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927241.1:n.3138T>A
XR_927242.1:n.3046T>A
XR_927241.2:n.3138T>A
XR_927242.2:n.3103T>A