Canonical Allele Identifier: CA603035651
Gene: ST14 HGNC NCBI

Linked Data

dbSNP Id: rs1164822619
gnomAD v2: 11-130079539-G-A
gnomAD v3: 11-130209644-G-A
gnomAD v4: 11-130209644-G-A
MyVariant Identifiers: chr11:g.130079539G>A (hg19) chr11:g.130209644G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130209644G>A , CM000673.2:g.130209644G>A GRCh38
NC_000011.9:g.130079539G>A , CM000673.1:g.130079539G>A GRCh37
NC_000011.8:g.129584749G>A NCBI36
NG_012132.1:g.54858G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000278742.6:c.2407-18G>A MANE Select ENSP00000278742.5:n.2407-18G>A
ENST00000278742.5:c.2407-18G>A ENSP00000278742.5:n.2407-18G>A
NM_021978.3:c.2407-18G>A NP_068813.1:n.2407-18G>A
NM_021978.4:c.2407-18G>A MANE Select NP_068813.1:n.2407-18G>A
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