Canonical Allele Identifier: CA595185089
Gene: STAMBPL1 HGNC NCBI
ACTA2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1187180870
gnomAD v2: 10-90694615-T-A
MyVariant Identifiers: chr10:g.90694615T>A (hg19) chr10:g.88934858T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.88934858T>A , CM000672.2:g.88934858T>A GRCh38
NC_000010.10:g.90694615T>A , CM000672.1:g.90694615T>A GRCh37
NC_000010.9:g.90684595T>A NCBI36
NG_011541.1:g.61533A>T , LRG_781:g.61533A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371927.7:c.1254+12422T>A (STAMBPL1) ENSP00000360995.3:n.1254+12422T>A
NR_125373.1:n.523-40T>A (ACTA2-AS1)
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