Canonical Allele Identifier: CA13153991

Gene: VSTM4

Linked Data

• dbSNP Id: rs2137920
• gnomAD v2: 10-50229638-T-A
• gnomAD v3: 10-49021593-T-A
• gnomAD v4: 10-49021593-T-A
• MyVariant Identifiers: chr10:g.50229638T>A (hg19) ; chr10:g.49021593T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49021593T>A , CM000672.2:g.49021593T>A	GRCh38
NC_000010.10:g.50229638T>A , CM000672.1:g.50229638T>A	GRCh37
NC_000010.9:g.49899644T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000332853.9:c.838-1818A>T MANE Select	ENSP00000331062.3:n.838-1818A>T
ENST00000332853.8:c.838-1818A>T	ENSP00000331062.3:n.838-1818A>T
NM_001031746.4:c.838-1818A>T	NP_001026916.2:n.838-1818A>T
XM_017015825.2:c.1049-1818A>T	XP_016871314.1:n.1049-1818A>T
XM_017015826.1:c.1034-1818A>T	XP_016871315.1:n.1034-1818A>T
XM_017015827.2:c.998-1818A>T	XP_016871316.1:n.998-1818A>T
XM_017015828.1:c.616-1818A>T	XP_016871317.1:n.616-1818A>T
XR_001747052.2:n.862-1818A>T
NM_001031746.5:c.838-1818A>T MANE Select	NP_001026916.2:n.838-1818A>T