Canonical Allele Identifier: CA2038861091
Gene: INHBC HGNC NCBI

Linked Data

dbSNP Id: rs1870684917
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57450273C>G , CM000674.2:g.57450273C>G GRCh38
NC_000012.11:g.57844056C>G , CM000674.1:g.57844056C>G GRCh37
NC_000012.10:g.56130323C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309668.3:c.*251C>G MANE Select ENSP00000308716.2:n.*251C>G
ENST00000309668.2:c.*251C>G ENSP00000308716.2:n.*251C>G
NM_005538.3:c.*251C>G NP_005529.1:n.*251C>G
NM_005538.4:c.*251C>G MANE Select NP_005529.1:n.*251C>G
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