Canonical Allele Identifier: CA2186761767
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72376071G= , CM000677.2:g.72376071G= GRCh38
NC_000015.9:g.72668412G= , CM000677.1:g.72668412G= GRCh37
NC_000015.8:g.70455466G= NCBI36
NG_009017.1:g.5109C=
NG_009017.2:g.5109C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268097.9:c.-99C= ENSP00000268097.5:n.-99C=
ENST00000569509.5:n.146+204C=
NM_000520.4:c.-99C= NP_000511.2:n.-99C=
NM_000520.5:c.-99C= NP_000511.2:n.-99C=
NM_001318825.1:c.-99C= NP_001305754.1:n.-99C=
NR_134869.1:n.403C=