Canonical Allele Identifier: CA435804564
Gene: INHCAP HGNC NCBI
TF HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.133410604T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133691760T>G , CM000665.2:g.133691760T>G GRCh38
NC_000003.11:g.133410604T>G , CM000665.1:g.133410604T>G GRCh37
NC_000003.10:g.134893294T>G NCBI36
NG_013080.2:g.34763T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000460564.5:n.209+3396T>G (INHCAP)
ENST00000475455.1:n.211T>G (INHCAP)
ENST00000490470.5:n.209+3396T>G (INHCAP)
ENST00000497521.5:n.208+3396T>G (INHCAP)
XM_011513100.1:c.-1289+3396T>G (TF) XP_011511402.1:n.-1289+3396T>G
NM_001354703.1:c.-940+3396T>G (TF) NP_001341632.1:n.-940+3396T>G
NM_001354703.2:c.-940+3396T>G (TF) NP_001341632.2:n.-940+3396T>G
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