Canonical Allele Identifier: CA2171795498
Gene: CHST14 HGNC NCBI

Linked Data

dbSNP Id: rs1566969394
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472359C>T , CM000677.2:g.40472359C>T GRCh38
NC_000015.9:g.40764558C>T , CM000677.1:g.40764558C>T GRCh37
NC_000015.8:g.38551850C>T NCBI36
NG_017074.1:g.6399C>T , LRG_600:g.6399C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*15C>T MANE Select ENSP00000307297.6:n.*15C>T
ENST00000306243.6:c.*15C>T ENSP00000307297.5:n.*15C>T
ENST00000559991.1:c.*15C>T ENSP00000453882.1:n.*15C>T
NM_130468.3:c.*15C>T , LRG_600t1:c.*15C>T NP_569735.1:n.*15C>T
NM_130468.4:c.*15C>T MANE Select NP_569735.1:n.*15C>T
Search 100 bp 5'
Search 100 bp 3'