Canonical Allele Identifier: CA1100605402
Gene: INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1784339840
gnomAD v3: 7-41772190-A-T
gnomAD v4: 7-41772190-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772190A>T , CM000669.2:g.41772190A>T GRCh38
NC_000007.13:g.41811788A>T , CM000669.1:g.41811788A>T GRCh37
NC_000007.12:g.41778313A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027118.1:n.359-706A>T
NR_027118.2:n.356-706A>T
XR_001745185.1:n.964+36476A>T
XR_001745186.1:n.954+36486A>T