Canonical Allele Identifier: CA573841912

Gene: INHBA-AS1

Linked Data

• dbSNP Id: rs1217324195
• gnomAD v2: 7-41811804-A-G
• gnomAD v3: 7-41772206-A-G
• gnomAD v4: 7-41772206-A-G
• MyVariant Identifiers: chr7:g.41811804A>G (hg19) ; chr7:g.41811804_41811805delinsGG (hg19) ; chr7:g.41772206A>G (hg38) ; chr7:g.41772206_41772207delinsGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41772206A>G , CM000669.2:g.41772206A>G	GRCh38
NC_000007.13:g.41811804A>G , CM000669.1:g.41811804A>G	GRCh37
NC_000007.12:g.41778329A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027118.1:n.359-690A>G
NR_027118.2:n.356-690A>G
XR_001745185.1:n.964+36492A>G
XR_001745186.1:n.954+36502A>G