Canonical Allele Identifier: CA435804635
Gene: INHCAP HGNC NCBI
TF HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.133410621C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133691777C>T , CM000665.2:g.133691777C>T GRCh38
NC_000003.11:g.133410621C>T , CM000665.1:g.133410621C>T GRCh37
NC_000003.10:g.134893311C>T NCBI36
NG_013080.2:g.34780C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000460564.5:n.209+3413C>T (INHCAP)
ENST00000475455.1:n.228C>T (INHCAP)
ENST00000490470.5:n.209+3413C>T (INHCAP)
ENST00000497521.5:n.208+3413C>T (INHCAP)
XM_011513100.1:c.-1289+3413C>T (TF) XP_011511402.1:n.-1289+3413C>T
NM_001354703.1:c.-940+3413C>T (TF) NP_001341632.1:n.-940+3413C>T
NM_001354703.2:c.-940+3413C>T (TF) NP_001341632.2:n.-940+3413C>T
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