Canonical Allele Identifier: CA211318136
Gene: STAMBPL1 HGNC NCBI
ACTA2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs983390127
gnomAD v4: 10-88935066-G-A
MyVariant Identifiers: chr10:g.90694823G>A (hg19) chr10:g.88935066G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.88935066G>A , CM000672.2:g.88935066G>A GRCh38
NC_000010.10:g.90694823G>A , CM000672.1:g.90694823G>A GRCh37
NC_000010.9:g.90684803G>A NCBI36
NG_011541.1:g.61325C>T , LRG_781:g.61325C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371927.7:c.1254+12630G>A (STAMBPL1) ENSP00000360995.3:n.1254+12630G>A
NR_125373.1:n.691G>A (ACTA2-AS1)
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