Canonical Allele Identifier: CA1500738163
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559899T= , CM000666.2:g.144559899T= GRCh38
NC_000004.11:g.145481051T= , CM000666.1:g.145481051T= GRCh37
NC_000004.10:g.145700501T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143921A= ENSP00000497507.1:n.328-143921A=
XR_939272.1:n.178+2085A=
XR_939273.1:n.178+2085A=
XR_939272.2:n.522+2085A=
XR_939273.2:n.522+2085A=