Canonical Allele Identifier: CA2636818716

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28370339T>A , CM000679.2:g.28370339T>A GRCh38
NC_000017.10:g.26697360T>A , CM000679.1:g.26697360T>A GRCh37
NC_000017.9:g.23721487T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226218.8:c.-136A>T (VTN) ENSP00000226218.4:n.-136A>T
ENST00000379061.8:n.170+5174T>A (SARM1)
ENST00000542029.1:c.-67-69A>T (VTN) ENSP00000440439.1:n.-67-69A>T
NM_000638.3:c.-136A>T (VTN) NP_000629.3:n.-136A>T