Canonical Allele Identifier: CA2629343925
Gene: HEXA HGNC NCBI

Linked Data

gnomAD v4: 15-72376046-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72376046T>G , CM000677.2:g.72376046T>G GRCh38
NC_000015.9:g.72668387T>G , CM000677.1:g.72668387T>G GRCh37
NC_000015.8:g.70455441T>G NCBI36
NG_009017.1:g.5134A>C
NG_009017.2:g.5134A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000268097.9:c.-74A>C ENSP00000268097.5:n.-74A>C
ENST00000569509.5:n.147-215A>C
NM_000520.4:c.-74A>C NP_000511.2:n.-74A>C
NM_000520.5:c.-74A>C NP_000511.2:n.-74A>C
NM_001318825.1:c.-74A>C NP_001305754.1:n.-74A>C
NR_134869.1:n.428A>C
Search 100 bp 5'
Search 100 bp 3'