Canonical Allele Identifier: CA470728072
Gene: STAMBPL1 HGNC NCBI
ACTA2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1198918087
gnomAD v4: 10-88934901-C-T
MyVariant Identifiers: chr10:g.90694658C>T (hg19) chr10:g.88934901C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.88934901C>T , CM000672.2:g.88934901C>T GRCh38
NC_000010.10:g.90694658C>T , CM000672.1:g.90694658C>T GRCh37
NC_000010.9:g.90684638C>T NCBI36
NG_011541.1:g.61490G>A , LRG_781:g.61490G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371927.7:c.1254+12465C>T (STAMBPL1) ENSP00000360995.3:n.1254+12465C>T
NR_125373.1:n.526C>T (ACTA2-AS1)
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