Canonical Allele Identifier: CA391767070
Gene: CHST14 HGNC NCBI

Linked Data

dbSNP Id: rs1285192331
gnomAD v2: 15-40764199-T-G
gnomAD v4: 15-40472000-T-G
MyVariant Identifiers: chr15:g.40764199T>G (hg19) chr15:g.40472000T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472000T>G , CM000677.2:g.40472000T>G GRCh38
NC_000015.9:g.40764199T>G , CM000677.1:g.40764199T>G GRCh37
NC_000015.8:g.38551491T>G NCBI36
NG_017074.1:g.6040T>G , LRG_600:g.6040T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000306243.7:c.787T>G MANE Select ENSP00000307297.6:p.Phe263Val
ENST00000306243.6:c.787T>G ENSP00000307297.5:p.Phe263Val
ENST00000559991.1:c.712T>G ENSP00000453882.1:p.Phe238Val
NM_130468.3:c.787T>G , LRG_600t1:c.787T>G NP_569735.1:p.Phe263Val
NM_130468.4:c.787T>G MANE Select NP_569735.1:p.Phe263Val
Search 100 bp 5'
Search 100 bp 3'