Canonical Allele Identifier: CA230708298
Gene: ST14 HGNC NCBI

Linked Data

dbSNP Id: rs999564248
gnomAD v3: 11-130209637-C-T
gnomAD v4: 11-130209637-C-T
MyVariant Identifiers: chr11:g.130079532C>T (hg19) chr11:g.130209637C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130209637C>T , CM000673.2:g.130209637C>T GRCh38
NC_000011.9:g.130079532C>T , CM000673.1:g.130079532C>T GRCh37
NC_000011.8:g.129584742C>T NCBI36
NG_012132.1:g.54851C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278742.6:c.2407-25C>T MANE Select ENSP00000278742.5:n.2407-25C>T
ENST00000278742.5:c.2407-25C>T ENSP00000278742.5:n.2407-25C>T
NM_021978.3:c.2407-25C>T NP_068813.1:n.2407-25C>T
NM_021978.4:c.2407-25C>T MANE Select NP_068813.1:n.2407-25C>T
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