Canonical Allele Identifier: CA230708331
Gene: ST14 HGNC NCBI

Linked Data

dbSNP Id: rs878909923
MyVariant Identifiers: chr11:g.130079546T>A (hg19) chr11:g.130209651T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130209651T>A , CM000673.2:g.130209651T>A GRCh38
NC_000011.9:g.130079546T>A , CM000673.1:g.130079546T>A GRCh37
NC_000011.8:g.129584756T>A NCBI36
NG_012132.1:g.54865T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000278742.6:c.2407-11T>A MANE Select ENSP00000278742.5:n.2407-11T>A
ENST00000278742.5:c.2407-11T>A ENSP00000278742.5:n.2407-11T>A
NM_021978.3:c.2407-11T>A NP_068813.1:n.2407-11T>A
NM_021978.4:c.2407-11T>A MANE Select NP_068813.1:n.2407-11T>A
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