Canonical Allele Identifier: CA470728427
Gene: STAMBPL1 HGNC NCBI
ACTA2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1251806223
gnomAD v2: 10-90694770-G-T
gnomAD v4: 10-88935013-G-T
MyVariant Identifiers: chr10:g.90694770G>T (hg19) chr10:g.88935013G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.88935013G>T , CM000672.2:g.88935013G>T GRCh38
NC_000010.10:g.90694770G>T , CM000672.1:g.90694770G>T GRCh37
NC_000010.9:g.90684750G>T NCBI36
NG_011541.1:g.61378C>A , LRG_781:g.61378C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371927.7:c.1254+12577G>T (STAMBPL1) ENSP00000360995.3:n.1254+12577G>T
NR_125373.1:n.638G>T (ACTA2-AS1)
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