Canonical Allele Identifier: CA1694877506
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24291872C= , CM000669.2:g.24291872C= GRCh38
NC_000007.13:g.24331491C= , CM000669.1:g.24331491C= GRCh37
NC_000007.12:g.24298016C= NCBI36
NG_016148.1:g.12685C=

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.41+27485G= XP_016868399.1:n.41+27485G=
XM_017012911.1:c.41+27485G= XP_016868400.1:n.41+27485G=
XR_001745121.1:n.473+27485G=
XR_001745122.1:n.345-94843G=
XR_001745123.1:n.473+27485G=
XR_001745124.1:n.473+27485G=
XR_001745125.1:n.473+27485G=
XR_001745126.1:n.473+27485G=
XR_001745127.1:n.345-36173G=
XR_001745129.1:n.473+27485G=
XR_001745130.1:n.473+27485G=
XR_001745131.1:n.473+27485G=
XR_001745132.1:n.473+27485G=