Canonical Allele Identifier: CA603035653
Gene: ST14 HGNC NCBI

Linked Data

dbSNP Id: rs1398605260
gnomAD v2: 11-130079545-G-C
gnomAD v4: 11-130209650-G-C
MyVariant Identifiers: chr11:g.130079545G>C (hg19) chr11:g.130209650G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130209650G>C , CM000673.2:g.130209650G>C GRCh38
NC_000011.9:g.130079545G>C , CM000673.1:g.130079545G>C GRCh37
NC_000011.8:g.129584755G>C NCBI36
NG_012132.1:g.54864G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000278742.6:c.2407-12G>C MANE Select ENSP00000278742.5:n.2407-12G>C
ENST00000278742.5:c.2407-12G>C ENSP00000278742.5:n.2407-12G>C
NM_021978.3:c.2407-12G>C NP_068813.1:n.2407-12G>C
NM_021978.4:c.2407-12G>C MANE Select NP_068813.1:n.2407-12G>C
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