Canonical Allele Identifier: CA435804482

Linked Data

MyVariant Identifiers: chr3:g.133410576G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133691732G>C , CM000665.2:g.133691732G>C GRCh38
NC_000003.11:g.133410576G>C , CM000665.1:g.133410576G>C GRCh37
NC_000003.10:g.134893266G>C NCBI36
NG_013080.2:g.34735G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000460564.5:n.209+3368G>C (INHCAP)
ENST00000475455.1:n.183G>C (INHCAP)
ENST00000490470.5:n.209+3368G>C (INHCAP)
ENST00000497521.5:n.208+3368G>C (INHCAP)
XM_011513100.1:c.-1289+3368G>C (TF) XP_011511402.1:n.-1289+3368G>C
NM_001354703.1:c.-940+3368G>C (TF) NP_001341632.1:n.-940+3368G>C
NM_001354703.2:c.-940+3368G>C (TF) NP_001341632.2:n.-940+3368G>C