Canonical Allele Identifier: CA996389103
Gene: HIF3A HGNC NCBI
gnomAD v4:

Genomic Alleles

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

Transcript Alleles

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