Canonical Allele Identifier: CA581633152

Gene: HGSNAT

Linked Data

• dbSNP Id: rs1300397959
• gnomAD v2: 8-42995602-G-A
• gnomAD v3: 8-43140459-G-A
• gnomAD v4: 8-43140459-G-A
• MyVariant Identifiers: chr8:g.42995602G>A (hg19) ; chr8:g.43140459G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140459G>A , CM000670.2:g.43140459G>A	GRCh38
NC_000008.10:g.42995602G>A , CM000670.1:g.42995602G>A	GRCh37
NC_000008.9:g.43114759G>A	NCBI36
NG_009552.1:g.5011G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.8:c.-38G>A	ENSP00000368965.4:n.-38G>A
NM_152419.2:c.-38G>A	NP_689632.2:n.-38G>A
XM_005273409.1:c.-38G>A	XP_005273466.1:n.-38G>A
XM_005273410.1:c.-38G>A	XP_005273467.1:n.-38G>A
XM_005273411.1:c.-38G>A	XP_005273468.1:n.-38G>A
XM_005273412.2:c.-38G>A	XP_005273469.1:n.-38G>A
XM_005273412.4:c.-38G>A	XP_005273469.1:n.-38G>A