Canonical Allele Identifier: CA851975171

Gene: HGSNAT

Linked Data

• dbSNP Id: rs1250825716
• MyVariant Identifiers: chr8:g.43055874T>C (hg19) ; chr8:g.43200731T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43200731T>C , CM000670.2:g.43200731T>C	GRCh38
NC_000008.10:g.43055874T>C , CM000670.1:g.43055874T>C	GRCh37
NC_000008.9:g.43175031T>C	NCBI36
NG_009552.1:g.65283T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.*1162T>C MANE Select	ENSP00000368965.4:n.*1162T>C
ENST00000379644.8:c.*1162T>C	ENSP00000368965.4:n.*1162T>C
NM_152419.2:c.*1162T>C	NP_689632.2:n.*1162T>C
XM_005273409.1:c.*1162T>C	XP_005273466.1:n.*1162T>C
XM_005273410.1:c.*1162T>C	XP_005273467.1:n.*1162T>C
XM_005273411.1:c.*1162T>C	XP_005273468.1:n.*1162T>C
NM_001363227.1:c.*1162T>C	NP_001350156.1:n.*1162T>C
NM_001363228.1:c.*1162T>C	NP_001350157.1:n.*1162T>C
NM_001363229.1:c.*1162T>C	NP_001350158.1:n.*1162T>C
NM_152419.3:c.*1162T>C MANE Select	NP_689632.2:n.*1162T>C
NM_001363227.2:c.*1162T>C	NP_001350156.1:n.*1162T>C
NM_001363228.2:c.*1162T>C	NP_001350157.1:n.*1162T>C
NM_001363229.2:c.*1162T>C	NP_001350158.1:n.*1162T>C