Canonical Allele Identifier: CA2008891756
Gene: ST14 HGNC NCBI

Linked Data

dbSNP Id: rs1953530272

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130209658C>T , CM000673.2:g.130209658C>T GRCh38
NC_000011.9:g.130079553C>T , CM000673.1:g.130079553C>T GRCh37
NC_000011.8:g.129584763C>T NCBI36
NG_012132.1:g.54872C>T

Transcript Alleles

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