Canonical Allele Identifier: CA1694872900
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24282697A= , CM000669.2:g.24282697A= GRCh38
NC_000007.13:g.24322316A= , CM000669.1:g.24322316A= GRCh37
NC_000007.12:g.24288841A= NCBI36
NG_016148.1:g.3510A=

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-26998T= XP_016868399.1:n.42-26998T=
XM_017012911.1:c.42-26998T= XP_016868400.1:n.42-26998T=
XR_001745121.1:n.473+36660T=
XR_001745122.1:n.345-85668T=
XR_001745123.1:n.473+36660T=
XR_001745124.1:n.473+36660T=
XR_001745125.1:n.473+36660T=
XR_001745126.1:n.473+36660T=
XR_001745127.1:n.345-26998T=
XR_001745129.1:n.473+36660T=
XR_001745130.1:n.473+36660T=
XR_001745131.1:n.473+36660T=
XR_001745132.1:n.473+36660T=