Canonical Allele Identifier: CA37542817
Gene: TGFB2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1249061
ClinVar RCV Id: RCV001654998
dbSNP Id: rs9331507
gnomAD v2: 1-218518422-GTCCT-G
gnomAD v3: 1-218345080-GTCCT-G
gnomAD v4: 1-218345080-GTCCT-G
MyVariant Identifiers: chr1:g.218518423_218518426del (hg19) chr1:g.218345081_218345084del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218345087_218345090del , CM000663.2:g.218345087_218345090del GRCh38
NC_000001.10:g.218518429_218518432del , CM000663.1:g.218518429_218518432del GRCh37
NC_000001.9:g.216585052_216585055del NCBI36
NG_027721.1:g.4754_4757del
NG_027721.2:g.4754_4757del

Transcript Alleles

HGVS Amino-acid Change
NR_046268.1:n.290+91_290+94del
Search 100 bp 5'
Search 100 bp 3'