Canonical Allele Identifier: CA2834184426
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559203G>A , CM000666.2:g.144559203G>A GRCh38
NC_000004.11:g.145480355G>A , CM000666.1:g.145480355G>A GRCh37
NC_000004.10:g.145699805G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143225C>T ENSP00000497507.1:n.328-143225C>T
XR_939272.1:n.178+2781C>T
XR_939273.1:n.178+2781C>T
XR_939272.2:n.522+2781C>T
XR_939273.2:n.522+2781C>T