Canonical Allele Identifier: CA838524724
Gene: INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1261996280
gnomAD v3: 7-41772277-A-G
gnomAD v4: 7-41772277-A-G
MyVariant Identifiers: chr7:g.41811875A>G (hg19) chr7:g.41772277A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772277A>G , CM000669.2:g.41772277A>G GRCh38
NC_000007.13:g.41811875A>G , CM000669.1:g.41811875A>G GRCh37
NC_000007.12:g.41778400A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027118.1:n.359-619A>G
NR_027118.2:n.356-619A>G
XR_001745185.1:n.964+36563A>G
XR_001745186.1:n.954+36573A>G
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