Canonical Allele Identifier: CA2633286889
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655556G>A , CM000678.2:g.55655556G>A GRCh38
NC_000016.9:g.55689468G>A , CM000678.1:g.55689468G>A GRCh37
NC_000016.8:g.54246969G>A NCBI36
NG_016969.1:g.4927G>A

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+43C>T