Canonical Allele Identifier: CA649096900
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559268T>A , CM000666.2:g.144559268T>A GRCh38
NC_000004.11:g.145480420T>A , CM000666.1:g.145480420T>A GRCh37
NC_000004.10:g.145699870T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143290A>T ENSP00000497507.1:n.328-143290A>T
XR_939272.1:n.178+2716A>T
XR_939273.1:n.178+2716A>T
XR_939272.2:n.522+2716A>T
XR_939273.2:n.522+2716A>T