Canonical Allele Identifier: CA1702561288
Gene: INHBA-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772263T= , CM000669.2:g.41772263T= GRCh38
NC_000007.13:g.41811861T= , CM000669.1:g.41811861T= GRCh37
NC_000007.12:g.41778386T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027118.1:n.359-633T=
NR_027118.2:n.356-633T=
XR_001745185.1:n.964+36549T=
XR_001745186.1:n.954+36559T=