Canonical Allele Identifier: CA13781920
Gene: SPATA13 HGNC NCBI

Linked Data

dbSNP Id: rs9805786
gnomAD v2: 13-24658356-G-T
gnomAD v3: 13-24084217-G-T
gnomAD v4: 13-24084217-G-T
MyVariant Identifiers: chr13:g.24658356G>T (hg19) chr13:g.24084217G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24084217G>T , CM000675.2:g.24084217G>T GRCh38
NC_000013.10:g.24658356G>T , CM000675.1:g.24658356G>T GRCh37
NC_000013.9:g.23556356G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000382141.4:c.-112+66516G>T ENSP00000371576.4:n.-112+66516G>T
ENST00000424834.6:c.-112+66516G>T ENSP00000398560.2:n.-112+66516G>T
NM_001286792.1:c.75+66516G>T NP_001273721.1:n.75+66516G>T
NM_001286792.2:c.75+66516G>T NP_001273721.1:n.75+66516G>T
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