Canonical Allele Identifier: CA2186761703
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72376021G= , CM000677.2:g.72376021G= GRCh38
NC_000015.9:g.72668362G= , CM000677.1:g.72668362G= GRCh37
NC_000015.8:g.70455416G= NCBI36
NG_009017.1:g.5159C=
NG_009017.2:g.5159C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268097.9:c.-49C= ENSP00000268097.5:n.-49C=
ENST00000569509.5:n.147-190C=
NM_000520.4:c.-49C= NP_000511.2:n.-49C=
NM_000520.5:c.-49C= NP_000511.2:n.-49C=
NM_001318825.1:c.-49C= NP_001305754.1:n.-49C=
NR_134869.1:n.453C=