Canonical Allele Identifier: CA157038713
Gene: INHBA-AS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10486722

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772310C>T , CM000669.2:g.41772310C>T GRCh38
NC_000007.12:g.41778433C>T NCBI36
NC_000007.13:g.41811908C>T , CM000669.1:g.41811908C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
NR_027118.1:n.359-586C>T