Canonical Allele Identifier: CA1694877529
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24291911C= , CM000669.2:g.24291911C= GRCh38
NC_000007.13:g.24331530C= , CM000669.1:g.24331530C= GRCh37
NC_000007.12:g.24298055C= NCBI36
NG_016148.1:g.12724C=

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.41+27446G= XP_016868399.1:n.41+27446G=
XM_017012911.1:c.41+27446G= XP_016868400.1:n.41+27446G=
XR_001745121.1:n.473+27446G=
XR_001745122.1:n.345-94882G=
XR_001745123.1:n.473+27446G=
XR_001745124.1:n.473+27446G=
XR_001745125.1:n.473+27446G=
XR_001745126.1:n.473+27446G=
XR_001745127.1:n.345-36212G=
XR_001745129.1:n.473+27446G=
XR_001745130.1:n.473+27446G=
XR_001745131.1:n.473+27446G=
XR_001745132.1:n.473+27446G=