Canonical Allele Identifier: CA176095853
Gene: HGSNAT HGNC NCBI

Linked Data

dbSNP Id: rs566748228
gnomAD v4: 8-43140451-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43140451G>T , CM000670.2:g.43140451G>T GRCh38
NC_000008.10:g.42995594G>T , CM000670.1:g.42995594G>T GRCh37
NC_000008.9:g.43114751G>T NCBI36
NG_009552.1:g.5003G>T

Transcript Alleles

HGVS Amino-acid Change
NM_152419.2:c.-46G>T NP_689632.2:n.-46G>T
XM_005273409.1:c.-46G>T XP_005273466.1:n.-46G>T
XM_005273410.1:c.-46G>T XP_005273467.1:n.-46G>T
XM_005273411.1:c.-46G>T XP_005273468.1:n.-46G>T
XM_005273412.2:c.-46G>T XP_005273469.1:n.-46G>T
XM_005273412.4:c.-46G>T XP_005273469.1:n.-46G>T