Canonical Allele Identifier: CA1702561249
Gene: INHBA-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772171T= , CM000669.2:g.41772171T= GRCh38
NC_000007.13:g.41811769T= , CM000669.1:g.41811769T= GRCh37
NC_000007.12:g.41778294T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027118.1:n.359-725T=
NR_027118.2:n.356-725T=
XR_001745185.1:n.964+36457T=
XR_001745186.1:n.954+36467T=