Canonical Allele Identifier: CA489764124
Gene: CHST14 HGNC NCBI

Linked Data

gnomAD v4: 15-40471297-C-G
MyVariant Identifiers: chr15:g.40763496C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40471297C>G , CM000677.2:g.40471297C>G GRCh38
NC_000015.9:g.40763496C>G , CM000677.1:g.40763496C>G GRCh37
NC_000015.8:g.38550788C>G NCBI36
NG_017074.1:g.5337C>G , LRG_600:g.5337C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.84C>G MANE Select ENSP00000307297.6:p.Gly28=
ENST00000306243.6:c.84C>G ENSP00000307297.5:p.Gly28=
ENST00000559991.1:c.84C>G ENSP00000453882.1:p.Gly28=
NM_130468.3:c.84C>G , LRG_600t1:c.84C>G NP_569735.1:p.Gly28=
NM_130468.4:c.84C>G MANE Select NP_569735.1:p.Gly28=
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