Canonical Allele Identifier: CA2579158849
Gene: HGSNAT HGNC NCBI

Linked Data

gnomAD v4: 8-43140455-G-A

Genomic Alleles

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

Transcript Alleles

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