Canonical Allele Identifier: CA1149396856
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036365G= , CM000663.2:g.2036365G= GRCh38
NC_000001.10:g.1967804G= , CM000663.1:g.1967804G= GRCh37
NC_000001.9:g.1957664G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.773+70C=
XR_001737845.2:n.846C=
XR_946823.3:n.776+70C=