Canonical Allele Identifier: CA15512476
Gene: INHBA HGNC NCBI
INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2877098
gnomAD v2: 7-41743294-T-C
gnomAD v3: 7-41703696-T-C
gnomAD v4: 7-41703696-T-C
MyVariant Identifiers: chr7:g.41743294T>C (hg19) chr7:g.41703696T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41703696T>C , CM000669.2:g.41703696T>C GRCh38
NC_000007.13:g.41743294T>C , CM000669.1:g.41743294T>C GRCh37
NC_000007.12:g.41709819T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000416150.1:n.52+1588A>G
ENST00000638023.1:c.-225-610A>G (INHBA) ENSP00000490646.1:n.-225-610A>G
NR_027118.1:n.174-6902T>C (INHBA-AS1)
NR_027119.1:n.142-6902T>C (INHBA-AS1)
NR_027118.2:n.171-6902T>C (INHBA-AS1)
NR_027119.2:n.171-6902T>C (INHBA-AS1)
XM_017012174.1:c.223+1588A>G (INHBA) XP_016867663.1:n.223+1588A>G
XM_017012175.1:c.29-3179A>G (INHBA) XP_016867664.1:n.29-3179A>G
XM_017012176.1:c.-144+1033A>G (INHBA) XP_016867665.1:n.-144+1033A>G
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