Canonical Allele Identifier: CA2739984307

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140463C>G , CM000670.2:g.43140463C>G	GRCh38
NC_000008.10:g.42995606C>G , CM000670.1:g.42995606C>G	GRCh37
NC_000008.9:g.43114763C>G	NCBI36
NG_009552.1:g.5015C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.8:c.-34C>G	ENSP00000368965.4:n.-34C>G
NM_152419.2:c.-34C>G	NP_689632.2:n.-34C>G
XM_005273409.1:c.-34C>G	XP_005273466.1:n.-34C>G
XM_005273410.1:c.-34C>G	XP_005273467.1:n.-34C>G
XM_005273411.1:c.-34C>G	XP_005273468.1:n.-34C>G
XM_005273412.2:c.-34C>G	XP_005273469.1:n.-34C>G
XM_005273412.4:c.-34C>G	XP_005273469.1:n.-34C>G