Canonical Allele Identifier: CA2815058696
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2674256C>A , CM000682.2:g.2674256C>A GRCh38
NC_000020.10:g.2654902C>A , CM000682.1:g.2654902C>A GRCh37
NC_000020.9:g.2602902C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937210.1:n.675-3816G>T
XR_937211.1:n.674-3673G>T
XR_937210.2:n.668-3816G>T
XR_937211.2:n.666-3673G>T