Canonical Allele Identifier: CA1044890065
Gene: OXTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8762739G>T , CM000665.2:g.8762739G>T GRCh38
NC_000003.11:g.8804425G>T , CM000665.1:g.8804425G>T GRCh37
NC_000003.10:g.8779425G>T NCBI36
NG_008797.2:g.33930G>T , LRG_329:g.33930G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000316793.8:c.922+4527C>A MANE Select ENSP00000324270.2:p.=
ENST00000316793.7:c.922+4527C>A ENSP00000324270.2:p.=
ENST00000472766.1:n.156-14738G>T
NM_000916.3:c.922+4527C>A NP_000907.2:p.=
XM_011533762.1:c.922+4527C>A XP_011532064.1:p.=
XM_011533763.1:c.922+4527C>A XP_011532065.1:p.=
NM_001354653.1:c.922+4527C>A NP_001341582.1:p.=
NM_001354654.1:c.922+4527C>A NP_001341583.1:p.=
NM_001354655.1:c.922+4527C>A NP_001341584.1:p.=
NM_001354656.1:c.922+4527C>A NP_001341585.1:p.=
NM_001354656.2:c.922+4527C>A NP_001341585.1:p.=
NM_000916.4:c.922+4527C>A MANE Select NP_000907.2:p.=
NM_001354653.2:c.922+4527C>A NP_001341582.1:p.=
NM_001354654.2:c.922+4527C>A NP_001341583.1:p.=
NM_001354655.2:c.922+4527C>A NP_001341584.1:p.=
NM_001354656.3:c.922+4527C>A NP_001341585.1:p.=