Canonical Allele Identifier: CA1694873587
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283983G= , CM000669.2:g.24283983G= GRCh38
NC_000007.13:g.24323602G= , CM000669.1:g.24323602G= GRCh37
NC_000007.12:g.24290127G= NCBI36
NG_016148.1:g.4796G=

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.42-28284C= XP_016868399.1:n.42-28284C=
XM_017012911.1:c.42-28284C= XP_016868400.1:n.42-28284C=
XR_001745121.1:n.473+35374C=
XR_001745122.1:n.345-86954C=
XR_001745123.1:n.473+35374C=
XR_001745124.1:n.473+35374C=
XR_001745125.1:n.473+35374C=
XR_001745126.1:n.473+35374C=
XR_001745127.1:n.345-28284C=
XR_001745129.1:n.473+35374C=
XR_001745130.1:n.473+35374C=
XR_001745131.1:n.473+35374C=
XR_001745132.1:n.473+35374C=