Canonical Allele Identifier: CA2633286832
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655467A>G , CM000678.2:g.55655467A>G GRCh38
NC_000016.9:g.55689379A>G , CM000678.1:g.55689379A>G GRCh37
NC_000016.8:g.54246880A>G NCBI36
NG_016969.1:g.4838A>G

Transcript Alleles

HGVS Amino-acid Change
XR_933603.1:n.54+132T>C