Canonical Allele Identifier: CA157038457
Gene: INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs916127342
MyVariant Identifiers: chr7:g.41772100G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772100G>C , CM000669.2:g.41772100G>C GRCh38
NC_000007.13:g.41811698G>C , CM000669.1:g.41811698G>C GRCh37
NC_000007.12:g.41778223G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027118.1:n.359-796G>C
NR_027118.2:n.356-796G>C
XR_001745185.1:n.964+36386G>C
XR_001745186.1:n.954+36396G>C
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