Canonical Allele Identifier: CA157038809
Gene: INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs749764852
gnomAD v2: 7-41812004-G-A
gnomAD v3: 7-41772406-G-A
gnomAD v4: 7-41772406-G-A
MyVariant Identifiers: chr7:g.41812004G>A (hg19) chr7:g.41772406G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772406G>A , CM000669.2:g.41772406G>A GRCh38
NC_000007.13:g.41812004G>A , CM000669.1:g.41812004G>A GRCh37
NC_000007.12:g.41778529G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027118.1:n.359-490G>A
NR_027118.2:n.356-490G>A
XR_001745185.1:n.964+36692G>A
XR_001745186.1:n.954+36702G>A
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