Canonical Allele Identifier: CA2636818739
Gene: VTN HGNC NCBI
SARM1 HGNC NCBI

Linked Data

gnomAD v4: 17-28370356-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28370356C>A , CM000679.2:g.28370356C>A GRCh38
NC_000017.10:g.26697377C>A , CM000679.1:g.26697377C>A GRCh37
NC_000017.9:g.23721504C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226218.8:c.-153G>T (VTN) ENSP00000226218.4:n.-153G>T
ENST00000379061.8:n.170+5191C>A (SARM1)
ENST00000542029.1:c.-67-86G>T (VTN) ENSP00000440439.1:n.-67-86G>T
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