Canonical Allele Identifier: CA1319876338
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198767760T= , CM000664.2:g.198767760T= GRCh38
NC_000002.11:g.199632484T= , CM000664.1:g.199632484T= GRCh37
NC_000002.10:g.199340729T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923758.1:n.72+4499A=
XR_923759.1:n.72+4499A=
XR_923760.1:n.72+4499A=
XR_923759.2:n.72+4499A=
XR_923760.2:n.72+4499A=