Canonical Allele Identifier: CA540837235

Linked Data

dbSNP Id: rs1296509047
gnomAD v2: 3-8813277-T-C
gnomAD v3: 3-8771591-T-C
gnomAD v4: 3-8771591-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771591T>C , CM000665.2:g.8771591T>C GRCh38
NC_000003.11:g.8813277T>C , CM000665.1:g.8813277T>C GRCh37
NC_000003.10:g.8788277T>C NCBI36
NG_008797.2:g.42782T>C , LRG_329:g.42782T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5886T>C (CAV3)
XM_011533763.1:c.-238-3000A>G (OXTR) XP_011532065.1:n.-238-3000A>G