Canonical Allele Identifier: CA211665922
Gene:

Linked Data

dbSNP Id: rs527597524
gnomAD v3: 10-94762431-T-A
gnomAD v4: 10-94762431-T-A
MyVariant Identifiers: chr10:g.96522188T>A (hg19) chr10:g.94762431T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762431T>A , CM000672.2:g.94762431T>A GRCh38
NC_000010.10:g.96522188T>A , CM000672.1:g.96522188T>A GRCh37
NC_000010.9:g.96512178T>A NCBI36
NG_008384.2:g.4726T>A
NG_008384.3:g.4751T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12627T>A ENSP00000483243.1:n.932-12627T>A
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