Canonical Allele Identifier: CA838524637

Gene: INHBA-AS1

Linked Data

• dbSNP Id: rs1451692646
• gnomAD v3: 7-41772142-A-C
• gnomAD v4: 7-41772142-A-C
• MyVariant Identifiers: chr7:g.41811740A>C (hg19) ; chr7:g.41772142A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41772142A>C , CM000669.2:g.41772142A>C	GRCh38
NC_000007.13:g.41811740A>C , CM000669.1:g.41811740A>C	GRCh37
NC_000007.12:g.41778265A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027118.1:n.359-754A>C
NR_027118.2:n.356-754A>C
XR_001745185.1:n.964+36428A>C
XR_001745186.1:n.954+36438A>C