Canonical Allele Identifier: CA2038861100
Gene: INHBC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57450281A= , CM000674.2:g.57450281A= GRCh38
NC_000012.11:g.57844064A= , CM000674.1:g.57844064A= GRCh37
NC_000012.10:g.56130331A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000309668.3:c.*259A= MANE Select ENSP00000308716.2:n.*259A=
ENST00000309668.2:c.*259A= ENSP00000308716.2:n.*259A=
NM_005538.3:c.*259A= NP_005529.1:n.*259A=
NM_005538.4:c.*259A= MANE Select NP_005529.1:n.*259A=
Search 100 bp 5'
Search 100 bp 3'