Canonical Allele Identifier: CA1044891394

Gene: OXTR CAV3

Linked Data

• dbSNP Id: rs1708616023
• gnomAD v3: 3-8766696-C-G
• gnomAD v4: 3-8766696-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8766696C>G , CM000665.2:g.8766696C>G	GRCh38
NC_000003.11:g.8808382C>G , CM000665.1:g.8808382C>G	GRCh37
NC_000003.10:g.8783382C>G	NCBI36
NG_008797.2:g.37887C>G , LRG_329:g.37887C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316793.8:c.922+570G>C (OXTR) MANE Select	ENSP00000324270.2:n.922+570G>C
ENST00000316793.7:c.922+570G>C (OXTR)	ENSP00000324270.2:n.922+570G>C
ENST00000472766.1:n.156-10781C>G (CAV3)
NM_000916.3:c.922+570G>C (OXTR)	NP_000907.2:n.922+570G>C
XM_011533762.1:c.922+570G>C (OXTR)	XP_011532064.1:n.922+570G>C
XM_011533763.1:c.922+570G>C (OXTR)	XP_011532065.1:n.922+570G>C
NM_001354653.1:c.922+570G>C (OXTR)	NP_001341582.1:n.922+570G>C
NM_001354654.1:c.922+570G>C (OXTR)	NP_001341583.1:n.922+570G>C
NM_001354655.1:c.922+570G>C (OXTR)	NP_001341584.1:n.922+570G>C
NM_001354656.1:c.922+570G>C (OXTR)	NP_001341585.1:n.922+570G>C
NM_001354656.2:c.922+570G>C (OXTR)	NP_001341585.1:n.922+570G>C
NM_000916.4:c.922+570G>C (OXTR) MANE Select	NP_000907.2:n.922+570G>C
NM_001354653.2:c.922+570G>C (OXTR)	NP_001341582.1:n.922+570G>C
NM_001354654.2:c.922+570G>C (OXTR)	NP_001341583.1:n.922+570G>C
NM_001354655.2:c.922+570G>C (OXTR)	NP_001341584.1:n.922+570G>C
NM_001354656.3:c.922+570G>C (OXTR)	NP_001341585.1:n.922+570G>C