Canonical Allele Identifier: CA2636818736

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28370353A>G , CM000679.2:g.28370353A>G GRCh38
NC_000017.10:g.26697374A>G , CM000679.1:g.26697374A>G GRCh37
NC_000017.9:g.23721501A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226218.8:c.-150T>C (VTN) ENSP00000226218.4:n.-150T>C
ENST00000379061.8:n.170+5188A>G (SARM1)
ENST00000542029.1:c.-67-83T>C (VTN) ENSP00000440439.1:n.-67-83T>C