Canonical Allele Identifier: CA371124714

Gene: HGSNAT

Linked Data

• dbSNP Id: rs1385070594
• gnomAD v2: 8-42995757-G-C
• gnomAD v4: 8-43140614-G-C
• MyVariant Identifiers: chr8:g.42995757G>C (hg19) ; chr8:g.43140614G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140614G>C , CM000670.2:g.43140614G>C	GRCh38
NC_000008.10:g.42995757G>C , CM000670.1:g.42995757G>C	GRCh37
NC_000008.9:g.43114914G>C	NCBI36
NG_009552.1:g.5166G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.118G>C MANE Select	ENSP00000368965.4:p.Asp40His
ENST00000379644.8:c.118G>C	ENSP00000368965.4:p.Asp40His
ENST00000517319.1:c.118G>C	ENSP00000430032.1:p.Asp40His
ENST00000520704.1:c.-33G>C	ENSP00000429109.1:n.-33G>C
NM_152419.2:c.118G>C	NP_689632.2:p.Asp40His
XM_005273409.1:c.118G>C	XP_005273466.1:p.Asp40His
XM_005273410.1:c.118G>C	XP_005273467.1:p.Asp40His
XM_005273411.1:c.118G>C	XP_005273468.1:p.Asp40His
XM_005273412.2:c.118G>C	XP_005273469.1:p.Asp40His
NM_001363227.1:c.118G>C	NP_001350156.1:p.Asp40His
NM_001363228.1:c.118G>C	NP_001350157.1:p.Asp40His
NM_001363229.1:c.-716G>C	NP_001350158.1:n.-716G>C
XM_005273412.4:c.118G>C	XP_005273469.1:p.Asp40His
NM_152419.3:c.118G>C MANE Select	NP_689632.2:p.Asp40His
NM_001363227.2:c.118G>C	NP_001350156.1:p.Asp40His
NM_001363228.2:c.118G>C	NP_001350157.1:p.Asp40His
NM_001363229.2:c.-716G>C	NP_001350158.1:n.-716G>C