Canonical Allele Identifier: CA11579895
Gene: OXTR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs237897
MyVariant Identifiers: chr3:g.8808285A>G (hg19) chr3:g.8766599A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8766599A>G , CM000665.2:g.8766599A>G GRCh38
NC_000003.10:g.8783285A>G NCBI36
NC_000003.11:g.8808285A>G , CM000665.1:g.8808285A>G GRCh37
NG_008797.2:g.37790A>G , LRG_329:g.37790A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000316793.7:c.922+667T>C ENSP00000324270.2:p.=
ENST00000472766.1:n.156-10878A>G
NM_000916.3:c.922+667T>C NP_000907.2:p.=
XM_011533762.1:c.922+667T>C XP_011532064.1:p.=
XM_011533763.1:c.922+667T>C XP_011532065.1:p.=