Canonical Allele Identifier: CA2581238119
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782414T>G , CM000677.2:g.95782414T>G GRCh38
NC_000015.9:g.96325643T>G , CM000677.1:g.96325643T>G GRCh37
NC_000015.8:g.94126647T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42775T>G