Canonical Allele Identifier: CA911552477

Linked Data

dbSNP Id: rs1314546592
gnomAD v3: 3-8762782-C-G
gnomAD v4: 3-8762782-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8762782C>G , CM000665.2:g.8762782C>G GRCh38
NC_000003.11:g.8804468C>G , CM000665.1:g.8804468C>G GRCh37
NC_000003.10:g.8779468C>G NCBI36
NG_008797.2:g.33973C>G , LRG_329:g.33973C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000316793.8:c.922+4484G>C (OXTR) MANE Select ENSP00000324270.2:n.922+4484G>C
ENST00000316793.7:c.922+4484G>C (OXTR) ENSP00000324270.2:n.922+4484G>C
ENST00000472766.1:n.156-14695C>G (CAV3)
NM_000916.3:c.922+4484G>C (OXTR) NP_000907.2:n.922+4484G>C
XM_011533762.1:c.922+4484G>C (OXTR) XP_011532064.1:n.922+4484G>C
XM_011533763.1:c.922+4484G>C (OXTR) XP_011532065.1:n.922+4484G>C
NM_001354653.1:c.922+4484G>C (OXTR) NP_001341582.1:n.922+4484G>C
NM_001354654.1:c.922+4484G>C (OXTR) NP_001341583.1:n.922+4484G>C
NM_001354655.1:c.922+4484G>C (OXTR) NP_001341584.1:n.922+4484G>C
NM_001354656.1:c.922+4484G>C (OXTR) NP_001341585.1:n.922+4484G>C
NM_001354656.2:c.922+4484G>C (OXTR) NP_001341585.1:n.922+4484G>C
NM_000916.4:c.922+4484G>C (OXTR) MANE Select NP_000907.2:n.922+4484G>C
NM_001354653.2:c.922+4484G>C (OXTR) NP_001341582.1:n.922+4484G>C
NM_001354654.2:c.922+4484G>C (OXTR) NP_001341583.1:n.922+4484G>C
NM_001354655.2:c.922+4484G>C (OXTR) NP_001341584.1:n.922+4484G>C
NM_001354656.3:c.922+4484G>C (OXTR) NP_001341585.1:n.922+4484G>C