Canonical Allele Identifier: CA2636818702

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28370330C>A , CM000679.2:g.28370330C>A GRCh38
NC_000017.10:g.26697351C>A , CM000679.1:g.26697351C>A GRCh37
NC_000017.9:g.23721478C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226218.8:c.-127G>T (VTN) ENSP00000226218.4:n.-127G>T
ENST00000379061.8:n.170+5165C>A (SARM1)
ENST00000542029.1:c.-67-60G>T (VTN) ENSP00000440439.1:n.-67-60G>T
NM_000638.3:c.-127G>T (VTN) NP_000629.3:n.-127G>T