Canonical Allele Identifier: CA911559071

Linked Data

dbSNP Id: rs1363179131

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771428T>C , CM000665.2:g.8771428T>C GRCh38
NC_000003.11:g.8813114T>C , CM000665.1:g.8813114T>C GRCh37
NC_000003.10:g.8788114T>C NCBI36
NG_008797.2:g.42619T>C , LRG_329:g.42619T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000472766.1:n.156-6049T>C (CAV3)
XM_011533763.1:c.-238-2837A>G (OXTR) XP_011532065.1:n.-238-2837A>G