Canonical Allele Identifier: CA157038686
Gene: INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs756487676
MyVariant Identifiers: chr7:g.41811884G>T (hg19) chr7:g.41772286G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772286G>T , CM000669.2:g.41772286G>T GRCh38
NC_000007.13:g.41811884G>T , CM000669.1:g.41811884G>T GRCh37
NC_000007.12:g.41778409G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027118.1:n.359-610G>T
NR_027118.2:n.356-610G>T
XR_001745185.1:n.964+36572G>T
XR_001745186.1:n.954+36582G>T
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