Canonical Allele Identifier: CA1702530723
Gene: INHBA HGNC NCBI
INHBA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2877098
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Genomic Alleles

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

Transcript Alleles

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