Canonical Allele Identifier: CA11436272

Linked Data

dbSNP Id: rs237889
gnomAD v2: 3-8802483-T-C
gnomAD v3: 3-8760797-T-C
gnomAD v4: 3-8760797-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8760797T>C , CM000665.2:g.8760797T>C GRCh38
NC_000003.11:g.8802483T>C , CM000665.1:g.8802483T>C GRCh37
NC_000003.10:g.8777483T>C NCBI36
NG_008797.2:g.31988T>C , LRG_329:g.31988T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000316793.8:c.922+6469A>G (OXTR) MANE Select ENSP00000324270.2:n.922+6469A>G
ENST00000316793.7:c.922+6469A>G (OXTR) ENSP00000324270.2:n.922+6469A>G
ENST00000472766.1:n.156-16680T>C (CAV3)
NM_000916.3:c.922+6469A>G (OXTR) NP_000907.2:n.922+6469A>G
XM_011533762.1:c.922+6469A>G (OXTR) XP_011532064.1:n.922+6469A>G
XM_011533763.1:c.922+6469A>G (OXTR) XP_011532065.1:n.922+6469A>G
NM_001354653.1:c.922+6469A>G (OXTR) NP_001341582.1:n.922+6469A>G
NM_001354654.1:c.922+6469A>G (OXTR) NP_001341583.1:n.922+6469A>G
NM_001354655.1:c.922+6469A>G (OXTR) NP_001341584.1:n.922+6469A>G
NM_001354656.1:c.922+6469A>G (OXTR) NP_001341585.1:n.922+6469A>G
NM_001354656.2:c.922+6469A>G (OXTR) NP_001341585.1:n.922+6469A>G
NM_000916.4:c.922+6469A>G (OXTR) MANE Select NP_000907.2:n.922+6469A>G
NM_001354653.2:c.922+6469A>G (OXTR) NP_001341582.1:n.922+6469A>G
NM_001354654.2:c.922+6469A>G (OXTR) NP_001341583.1:n.922+6469A>G
NM_001354655.2:c.922+6469A>G (OXTR) NP_001341584.1:n.922+6469A>G
NM_001354656.3:c.922+6469A>G (OXTR) NP_001341585.1:n.922+6469A>G