Canonical Allele Identifier: CA2636818713

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28370337G>T , CM000679.2:g.28370337G>T GRCh38
NC_000017.10:g.26697358G>T , CM000679.1:g.26697358G>T GRCh37
NC_000017.9:g.23721485G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226218.8:c.-134C>A (VTN) ENSP00000226218.4:n.-134C>A
ENST00000379061.8:n.170+5172G>T (SARM1)
ENST00000542029.1:c.-67-67C>A (VTN) ENSP00000440439.1:n.-67-67C>A
NM_000638.3:c.-134C>A (VTN) NP_000629.3:n.-134C>A