Canonical Allele Identifier: CA1044892291

Gene: OXTR CAV3

Linked Data

• dbSNP Id: rs1708703998
• gnomAD v3: 3-8768977-T-C
• gnomAD v4: 3-8768977-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8768977T>C , CM000665.2:g.8768977T>C	GRCh38
NC_000003.11:g.8810663T>C , CM000665.1:g.8810663T>C	GRCh37
NC_000003.10:g.8785663T>C	NCBI36
NG_008797.2:g.40168T>C , LRG_329:g.40168T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316793.8:c.-239+254A>G (OXTR) MANE Select	ENSP00000324270.2:n.-239+254A>G
ENST00000316793.7:c.-239+254A>G (OXTR)	ENSP00000324270.2:n.-239+254A>G
ENST00000431493.1:c.-239+277A>G (OXTR)	ENSP00000414828.1:n.-239+277A>G
ENST00000472766.1:n.156-8500T>C (CAV3)
ENST00000474615.1:n.383+254A>G (OXTR)
NM_000916.3:c.-239+254A>G (OXTR)	NP_000907.2:n.-239+254A>G
XM_011533762.1:c.-239+277A>G (OXTR)	XP_011532064.1:n.-239+277A>G
XM_011533763.1:c.-238-386A>G (OXTR)	XP_011532065.1:n.-238-386A>G
NM_001354653.1:c.-239+254A>G (OXTR)	NP_001341582.1:n.-239+254A>G
NM_001354654.1:c.-239+277A>G (OXTR)	NP_001341583.1:n.-239+277A>G
NM_001354655.1:c.-239+71A>G (OXTR)	NP_001341584.1:n.-239+71A>G
NM_000916.4:c.-239+254A>G (OXTR) MANE Select	NP_000907.2:n.-239+254A>G
NM_001354653.2:c.-239+254A>G (OXTR)	NP_001341582.1:n.-239+254A>G
NM_001354654.2:c.-239+277A>G (OXTR)	NP_001341583.1:n.-239+277A>G
NM_001354655.2:c.-239+71A>G (OXTR)	NP_001341584.1:n.-239+71A>G