Canonical Allele Identifier: CA573841913
Gene: INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1562597311
gnomAD v2: 7-41811804-AG-A
gnomAD v3: 7-41772206-AG-A
gnomAD v4: 7-41772206-AG-A
MyVariant Identifiers: chr7:g.41811805del (hg19) chr7:g.41772207del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41772208del , CM000669.2:g.41772208del GRCh38
NC_000007.13:g.41811806del , CM000669.1:g.41811806del GRCh37
NC_000007.12:g.41778331del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027118.1:n.359-688del
NR_027118.2:n.356-688del
XR_001745185.1:n.964+36494del
XR_001745186.1:n.954+36504del
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