Canonical Allele Identifier: CA7481703
Gene: CHST14 HGNC NCBI

Linked Data

dbSNP Id: rs76922844
ExAC: 15:40764540 G / A
gnomAD v2: 15-40764540-G-A
gnomAD v4: 15-40472341-G-A
MyVariant Identifiers: chr15:g.40764540G>A (hg19) chr15:g.40472341G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472341G>A , CM000677.2:g.40472341G>A GRCh38
NC_000015.9:g.40764540G>A , CM000677.1:g.40764540G>A GRCh37
NC_000015.8:g.38551832G>A NCBI36
NG_017074.1:g.6381G>A , LRG_600:g.6381G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1128G>A MANE Select ENSP00000307297.6:p.Gln376=
ENST00000306243.6:c.1128G>A ENSP00000307297.5:p.Gln376=
ENST00000559991.1:c.1053G>A ENSP00000453882.1:p.Gln351=
NM_130468.3:c.1128G>A , LRG_600t1:c.1128G>A NP_569735.1:p.Gln376=
NM_130468.4:c.1128G>A MANE Select NP_569735.1:p.Gln376=
Search 100 bp 5'
Search 100 bp 3'