Canonical Allele Identifier: CA2780586690
Gene: GGH HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039044A>T , CM000670.2:g.63039044A>T GRCh38
NC_000008.10:g.63951603A>T , CM000670.1:g.63951603A>T GRCh37
NC_000008.9:g.64114157A>T NCBI36
NG_028126.1:g.5008T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.364T>A
ENST00000679326.1:c.-276T>A ENSP00000504262.1:n.-276T>A
ENST00000260118.6:c.-276T>A ENSP00000260118.6:n.-276T>A
NM_003878.2:c.-276T>A NP_003869.1:n.-276T>A
XM_011517623.1:c.-276T>A XP_011515925.1:n.-276T>A
Search 100 bp 5'
Search 100 bp 3'