Canonical Allele Identifier: CA435804840
Gene: INHCAP HGNC NCBI
TF HGNC NCBI

Linked Data

gnomAD v4: 3-133691823-C-A
MyVariant Identifiers: chr3:g.133410667C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133691823C>A , CM000665.2:g.133691823C>A GRCh38
NC_000003.11:g.133410667C>A , CM000665.1:g.133410667C>A GRCh37
NC_000003.10:g.134893357C>A NCBI36
NG_013080.2:g.34826C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000460564.5:n.209+3459C>A (INHCAP)
ENST00000475455.1:n.274C>A (INHCAP)
ENST00000490470.5:n.209+3459C>A (INHCAP)
ENST00000497521.5:n.208+3459C>A (INHCAP)
XM_011513100.1:c.-1289+3459C>A (TF) XP_011511402.1:n.-1289+3459C>A
NM_001354703.1:c.-940+3459C>A (TF) NP_001341632.1:n.-940+3459C>A
NM_001354703.2:c.-940+3459C>A (TF) NP_001341632.2:n.-940+3459C>A
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