Canonical Allele Identifier: CA1788923497
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038947T= , CM000670.2:g.63038947T= GRCh38
NC_000008.10:g.63951506T= , CM000670.1:g.63951506T= GRCh37
NC_000008.9:g.64114060T= NCBI36
NG_028126.1:g.5105A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.461A=
ENST00000679326.1:c.-179A= ENSP00000504262.1:n.-179A=
ENST00000260118.6:c.-179A= ENSP00000260118.6:n.-179A=
NM_003878.2:c.-179A= NP_003869.1:n.-179A=
XM_011517623.1:c.-179A= XP_011515925.1:n.-179A=