Canonical Allele Identifier: CA6364396
Gene: ST14 HGNC NCBI

Linked Data

dbSNP Id: rs757034861

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130209634A>G , CM000673.2:g.130209634A>G GRCh38
NC_000011.9:g.130079529A>G , CM000673.1:g.130079529A>G GRCh37
NC_000011.8:g.129584739A>G NCBI36
NG_012132.1:g.54848A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000278742.6:c.2407-28A>G MANE Select ENSP00000278742.5:n.2407-28A>G
ENST00000278742.5:c.2407-28A>G ENSP00000278742.5:n.2407-28A>G
NM_021978.3:c.2407-28A>G NP_068813.1:n.2407-28A>G
NM_021978.4:c.2407-28A>G MANE Select NP_068813.1:n.2407-28A>G