Canonical Allele Identifier: CA2038861089
Gene: INHBC HGNC NCBI

Linked Data

dbSNP Id: rs1870684847
gnomAD v4: 12-57450272-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57450272C>T , CM000674.2:g.57450272C>T GRCh38
NC_000012.11:g.57844055C>T , CM000674.1:g.57844055C>T GRCh37
NC_000012.10:g.56130322C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000309668.3:c.*250C>T MANE Select ENSP00000308716.2:n.*250C>T
ENST00000309668.2:c.*250C>T ENSP00000308716.2:n.*250C>T
NM_005538.3:c.*250C>T NP_005529.1:n.*250C>T
NM_005538.4:c.*250C>T MANE Select NP_005529.1:n.*250C>T
Search 100 bp 5'
Search 100 bp 3'