Canonical Allele Identifier: CA13240533
Gene:

Linked Data

dbSNP Id: rs1144520
gnomAD v2: 10-29386013-T-A
gnomAD v3: 10-29097084-T-A
gnomAD v4: 10-29097084-T-A
MyVariant Identifiers: chr10:g.29386013T>A (hg19) chr10:g.29097084T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29097084T>A , CM000672.2:g.29097084T>A GRCh38
NC_000010.10:g.29386013T>A , CM000672.1:g.29386013T>A GRCh37
NC_000010.9:g.29426019T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001747285.1:n.89-234T>A
XR_001747286.1:n.89-234T>A
Search 100 bp 5'
Search 100 bp 3'