Canonical Allele Identifier: CA157038536
Gene: INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1039452664
MyVariant Identifiers: chr7:g.41811748G>A (hg19) chr7:g.41772150G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772150G>A , CM000669.2:g.41772150G>A GRCh38
NC_000007.13:g.41811748G>A , CM000669.1:g.41811748G>A GRCh37
NC_000007.12:g.41778273G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027118.1:n.359-746G>A
NR_027118.2:n.356-746G>A
XR_001745185.1:n.964+36436G>A
XR_001745186.1:n.954+36446G>A
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