Canonical Allele Identifier: CA14462460

Gene: VTN SARM1

Linked Data

• dbSNP Id: rs2227721
• gnomAD v2: 17-26697451-C-A
• gnomAD v3: 17-28370430-C-A
• gnomAD v4: 17-28370430-C-A
• MyVariant Identifiers: chr17:g.26697451C>A (hg19) ; chr17:g.28370430C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28370430C>A , CM000679.2:g.28370430C>A	GRCh38
NC_000017.10:g.26697451C>A , CM000679.1:g.26697451C>A	GRCh37
NC_000017.9:g.23721578C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000226218.8:c.-227G>T (VTN)	ENSP00000226218.4:n.-227G>T
ENST00000379061.8:n.170+5265C>A (SARM1)
ENST00000542029.1:c.-67-160G>T (VTN)	ENSP00000440439.1:n.-67-160G>T