Canonical Allele Identifier: CA1788923539
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038994C= , CM000670.2:g.63038994C= GRCh38
NC_000008.10:g.63951553C= , CM000670.1:g.63951553C= GRCh37
NC_000008.9:g.64114107C= NCBI36
NG_028126.1:g.5058G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.414G=
ENST00000679326.1:c.-226G= ENSP00000504262.1:n.-226G=
ENST00000260118.6:c.-226G= ENSP00000260118.6:n.-226G=
NM_003878.2:c.-226G= NP_003869.1:n.-226G=
XM_011517623.1:c.-226G= XP_011515925.1:n.-226G=