Canonical Allele Identifier: CA1149396967
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036483G= , CM000663.2:g.2036483G= GRCh38
NC_000001.10:g.1967922G= , CM000663.1:g.1967922G= GRCh37
NC_000001.9:g.1957782G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.725C=
XR_001737845.2:n.728C=
XR_946823.3:n.728C=