Canonical Allele Identifier: CA1500737449
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559187T= , CM000666.2:g.144559187T= GRCh38
NC_000004.11:g.145480339T= , CM000666.1:g.145480339T= GRCh37
NC_000004.10:g.145699789T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143209A= ENSP00000497507.1:n.328-143209A=
XR_939272.1:n.178+2797A=
XR_939273.1:n.178+2797A=
XR_939272.2:n.522+2797A=
XR_939273.2:n.522+2797A=