Canonical Allele Identifier: CA16618645
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 422050
ClinVar RCV Id: RCV000478090 RCV000626050
dbSNP Id: rs1064795522
gnomAD v4: 8-43192320-G-T
MyVariant Identifiers: chr8:g.43047463G>T (hg19) chr8:g.43192320G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43192320G>T , CM000670.2:g.43192320G>T GRCh38
NC_000008.10:g.43047463G>T , CM000670.1:g.43047463G>T GRCh37
NC_000008.9:g.43166620G>T NCBI36
NG_009552.1:g.56872G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379644.9:c.1267G>T MANE Select ENSP00000368965.4:p.Gly423Trp
ENST00000379644.8:c.1267G>T ENSP00000368965.4:p.Gly423Trp
ENST00000520678.1:n.200G>T
ENST00000521576.1:c.418G>T ENSP00000429029.1:p.Gly140Trp
ENST00000524016.5:c.371G>T
NM_152419.2:c.1267G>T NP_689632.2:p.Gly423Trp
XM_005273409.1:c.1267G>T XP_005273466.1:p.Gly423Trp
XM_005273410.1:c.1267G>T XP_005273467.1:p.Gly423Trp
XM_005273411.1:c.1075G>T XP_005273468.1:p.Gly359Trp
XM_005273412.2:c.1267G>T XP_005273469.1:p.Gly423Trp
NM_001363227.1:c.1267G>T NP_001350156.1:p.Gly423Trp
NM_001363228.1:c.1075G>T NP_001350157.1:p.Gly359Trp
NM_001363229.1:c.403G>T NP_001350158.1:p.Gly135Trp
XM_005273412.4:c.1267G>T XP_005273469.1:p.Gly423Trp
NM_152419.3:c.1267G>T MANE Select NP_689632.2:p.Gly423Trp
NM_001363227.2:c.1267G>T NP_001350156.1:p.Gly423Trp
NM_001363228.2:c.1075G>T NP_001350157.1:p.Gly359Trp
NM_001363229.2:c.403G>T NP_001350158.1:p.Gly135Trp
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