Canonical Allele Identifier: CA1100605472
Gene: INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1784342968
gnomAD v3: 7-41772398-G-A
gnomAD v4: 7-41772398-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772398G>A , CM000669.2:g.41772398G>A GRCh38
NC_000007.13:g.41811996G>A , CM000669.1:g.41811996G>A GRCh37
NC_000007.12:g.41778521G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027118.1:n.359-498G>A
NR_027118.2:n.356-498G>A
XR_001745185.1:n.964+36684G>A
XR_001745186.1:n.954+36694G>A
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