Canonical Allele Identifier: CA157038561
Gene: INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs888307174
gnomAD v3: 7-41772187-A-G
gnomAD v4: 7-41772187-A-G
MyVariant Identifiers: chr7:g.41811785A>G (hg19) chr7:g.41772187A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772187A>G , CM000669.2:g.41772187A>G GRCh38
NC_000007.13:g.41811785A>G , CM000669.1:g.41811785A>G GRCh37
NC_000007.12:g.41778310A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027118.1:n.359-709A>G
NR_027118.2:n.356-709A>G
XR_001745185.1:n.964+36473A>G
XR_001745186.1:n.954+36483A>G
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