Canonical Allele Identifier: CA2739984304
Gene: HGSNAT HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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