Canonical Allele Identifier: CA1941456007
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122458385A= , CM000672.2:g.122458385A= GRCh38
NC_000010.10:g.124217901A= , CM000672.1:g.124217901A= GRCh37
NC_000010.9:g.124207891A= NCBI36
NG_011554.1:g.1861A=
NG_011725.1:g.8723A=

Transcript Alleles

HGVS Amino-acid Change
XR_946382.1:n.1827+110T=
XR_946383.1:n.1827+110T=
XR_946384.1:n.1576+110T=
XR_946385.1:n.1827+110T=
XR_946382.2:n.1855+110T=
XR_946383.2:n.1855+110T=
XR_946384.2:n.1580+110T=
XR_946385.2:n.1855+110T=