Canonical Allele Identifier: CA838524783

Gene: INHBA-AS1

Linked Data

• dbSNP Id: rs1461351361
• gnomAD v3: 7-41772371-T-C
• gnomAD v4: 7-41772371-T-C
• MyVariant Identifiers: chr7:g.41811969T>C (hg19) ; chr7:g.41772371T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41772371T>C , CM000669.2:g.41772371T>C	GRCh38
NC_000007.13:g.41811969T>C , CM000669.1:g.41811969T>C	GRCh37
NC_000007.12:g.41778494T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027118.1:n.359-525T>C
NR_027118.2:n.356-525T>C
XR_001745185.1:n.964+36657T>C
XR_001745186.1:n.954+36667T>C