Canonical Allele Identifier: CA1779749621
Gene: HGSNAT HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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