Canonical Allele Identifier: CA69851504
Gene: OXTR HGNC NCBI

Linked Data

dbSNP Id: rs770520799

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8762850C>G , CM000665.2:g.8762850C>G GRCh38
NC_000003.11:g.8804536C>G , CM000665.1:g.8804536C>G GRCh37
NC_000003.10:g.8779536C>G NCBI36
NG_008797.2:g.34041C>G , LRG_329:g.34041C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000316793.8:c.922+4416G>C MANE Select ENSP00000324270.2:p.=
ENST00000316793.7:c.922+4416G>C ENSP00000324270.2:p.=
ENST00000472766.1:n.156-14627C>G
NM_000916.3:c.922+4416G>C NP_000907.2:p.=
XM_011533762.1:c.922+4416G>C XP_011532064.1:p.=
XM_011533763.1:c.922+4416G>C XP_011532065.1:p.=
NM_001354653.1:c.922+4416G>C NP_001341582.1:p.=
NM_001354654.1:c.922+4416G>C NP_001341583.1:p.=
NM_001354655.1:c.922+4416G>C NP_001341584.1:p.=
NM_001354656.1:c.922+4416G>C NP_001341585.1:p.=
NM_001354656.2:c.922+4416G>C NP_001341585.1:p.=
NM_000916.4:c.922+4416G>C MANE Select NP_000907.2:p.=
NM_001354653.2:c.922+4416G>C NP_001341582.1:p.=
NM_001354654.2:c.922+4416G>C NP_001341583.1:p.=
NM_001354655.2:c.922+4416G>C NP_001341584.1:p.=
NM_001354656.3:c.922+4416G>C NP_001341585.1:p.=