Canonical Allele Identifier: CA971332823
Gene: HEXA HGNC NCBI

Linked Data

dbSNP Id: rs2089065422

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72376070G>A , CM000677.2:g.72376070G>A GRCh38
NC_000015.9:g.72668411G>A , CM000677.1:g.72668411G>A GRCh37
NC_000015.8:g.70455465G>A NCBI36
NG_009017.1:g.5110C>T
NG_009017.2:g.5110C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000268097.9:c.-98C>T ENSP00000268097.5:n.-98C>T
ENST00000569509.5:n.146+205C>T
NM_000520.4:c.-98C>T NP_000511.2:n.-98C>T
NM_000520.5:c.-98C>T NP_000511.2:n.-98C>T
NM_001318825.1:c.-98C>T NP_001305754.1:n.-98C>T
NR_134869.1:n.404C>T