Canonical Allele Identifier: CA14644706
Gene: HIF3A HGNC NCBI
COSMIC:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.46297176G>A , CM000681.2:g.46297176G>A GRCh38
NC_000019.9:g.46800433G>A , CM000681.1:g.46800433G>A GRCh37
NC_000019.8:g.51492273G>A NCBI36
NG_029679.1:g.5129G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377670.9:c.26+74G>A MANE Select ENSP00000366898.3:n.26+74G>A
ENST00000244302.8:n.57+74G>A
ENST00000377670.8:c.26+74G>A ENSP00000366898.3:n.26+74G>A
ENST00000475432.6:n.57+74G>A
ENST00000533789.5:c.26+74G>A ENSP00000432809.1:n.26+74G>A
NM_152795.3:c.26+74G>A NP_690008.2:n.26+74G>A
XM_005259152.3:c.26+74G>A XP_005259209.1:n.26+74G>A
XM_005259155.3:c.26+74G>A XP_005259212.1:n.26+74G>A
XM_005259156.3:c.26+74G>A XP_005259213.1:n.26+74G>A
XM_006723325.1:c.-36+74G>A XP_006723388.1:n.-36+74G>A
XR_935849.1:n.54+74G>A
XM_005259152.4:c.26+74G>A XP_005259209.1:n.26+74G>A
XM_005259155.4:c.26+74G>A XP_005259212.1:n.26+74G>A
XM_005259156.4:c.26+74G>A XP_005259213.1:n.26+74G>A
XM_017027132.1:c.26+74G>A XP_016882621.1:n.26+74G>A
XM_017027133.1:c.26+74G>A XP_016882622.1:n.26+74G>A
XM_017027134.1:c.26+74G>A XP_016882623.1:n.26+74G>A
XM_017027136.1:c.26+74G>A XP_016882625.1:n.26+74G>A
XM_017027138.1:c.26+74G>A XP_016882627.1:n.26+74G>A
XM_017027140.1:c.-36+74G>A XP_016882629.1:n.-36+74G>A
XR_001753736.1:n.53+74G>A
XR_002958343.1:n.53+74G>A
XR_935849.2:n.53+74G>A
NM_152795.4:c.26+74G>A MANE Select NP_690008.2:n.26+74G>A