Canonical Allele Identifier: CA838524646
Gene: INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1186881140
gnomAD v3: 7-41772164-T-G
gnomAD v4: 7-41772164-T-G
MyVariant Identifiers: chr7:g.41811762T>G (hg19) chr7:g.41772164T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772164T>G , CM000669.2:g.41772164T>G GRCh38
NC_000007.13:g.41811762T>G , CM000669.1:g.41811762T>G GRCh37
NC_000007.12:g.41778287T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027118.1:n.359-732T>G
NR_027118.2:n.356-732T>G
XR_001745185.1:n.964+36450T>G
XR_001745186.1:n.954+36460T>G
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