Canonical Allele Identifier: CA1140474065
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682245G= , CM000663.2:g.213682245G= GRCh38
NC_000001.10:g.213855588G= , CM000663.1:g.213855588G= GRCh37
NC_000001.9:g.211922211G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738463.1:n.601-49172G=
XR_001738464.1:n.426-49172G=