Canonical Allele Identifier: CA157038563
Gene: INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs191630887
gnomAD v2: 7-41811798-C-A
gnomAD v3: 7-41772200-C-A
gnomAD v4: 7-41772200-C-A
MyVariant Identifiers: chr7:g.41811798C>A (hg19) chr7:g.41772200C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772200C>A , CM000669.2:g.41772200C>A GRCh38
NC_000007.13:g.41811798C>A , CM000669.1:g.41811798C>A GRCh37
NC_000007.12:g.41778323C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027118.1:n.359-696C>A
NR_027118.2:n.356-696C>A
XR_001745185.1:n.964+36486C>A
XR_001745186.1:n.954+36496C>A
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