Canonical Allele Identifier: CA2627823836
Gene: CHST14 HGNC NCBI

Linked Data

gnomAD v4: 15-40471189-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40471189C>G , CM000677.2:g.40471189C>G GRCh38
NC_000015.9:g.40763388C>G , CM000677.1:g.40763388C>G GRCh37
NC_000015.8:g.38550680C>G NCBI36
NG_017074.1:g.5229C>G , LRG_600:g.5229C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.-25C>G MANE Select ENSP00000307297.6:n.-25C>G
ENST00000306243.6:c.-25C>G ENSP00000307297.5:n.-25C>G
ENST00000559991.1:c.-25C>G ENSP00000453882.1:n.-25C>G
NM_130468.3:c.-25C>G , LRG_600t1:c.-25C>G NP_569735.1:n.-25C>G
NM_130468.4:c.-25C>G MANE Select NP_569735.1:n.-25C>G
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