Canonical Allele Identifier: CA1344418085

Linked Data

dbSNP Id: rs1708755991

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771653A>T , CM000665.2:g.8771653A>T GRCh38
NC_000003.11:g.8813339A>T , CM000665.1:g.8813339A>T GRCh37
NC_000003.10:g.8788339A>T NCBI36
NG_008797.2:g.42844A>T , LRG_329:g.42844A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5824A>T (CAV3)
XM_011533763.1:c.-238-3062T>A (OXTR) XP_011532065.1:n.-238-3062T>A