Canonical Allele Identifier: CA237770609
Gene: INHBC HGNC NCBI

Linked Data

dbSNP Id: rs543821071
gnomAD v3: 12-57450267-G-A
gnomAD v4: 12-57450267-G-A
MyVariant Identifiers: chr12:g.57844050G>A (hg19) chr12:g.57450267G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57450267G>A , CM000674.2:g.57450267G>A GRCh38
NC_000012.11:g.57844050G>A , CM000674.1:g.57844050G>A GRCh37
NC_000012.10:g.56130317G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000309668.3:c.*245G>A MANE Select ENSP00000308716.2:n.*245G>A
ENST00000309668.2:c.*245G>A ENSP00000308716.2:n.*245G>A
NM_005538.3:c.*245G>A NP_005529.1:n.*245G>A
NM_005538.4:c.*245G>A MANE Select NP_005529.1:n.*245G>A
Search 100 bp 5'
Search 100 bp 3'