Canonical Allele Identifier: CA2739984302

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140455G>C , CM000670.2:g.43140455G>C	GRCh38
NC_000008.10:g.42995598G>C , CM000670.1:g.42995598G>C	GRCh37
NC_000008.9:g.43114755G>C	NCBI36
NG_009552.1:g.5007G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.8:c.-42G>C	ENSP00000368965.4:n.-42G>C
NM_152419.2:c.-42G>C	NP_689632.2:n.-42G>C
XM_005273409.1:c.-42G>C	XP_005273466.1:n.-42G>C
XM_005273410.1:c.-42G>C	XP_005273467.1:n.-42G>C
XM_005273411.1:c.-42G>C	XP_005273468.1:n.-42G>C
XM_005273412.2:c.-42G>C	XP_005273469.1:n.-42G>C
XM_005273412.4:c.-42G>C	XP_005273469.1:n.-42G>C