Canonical Allele Identifier: CA1788923500
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038950G= , CM000670.2:g.63038950G= GRCh38
NC_000008.10:g.63951509G= , CM000670.1:g.63951509G= GRCh37
NC_000008.9:g.64114063G= NCBI36
NG_028126.1:g.5102C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.458C=
ENST00000679326.1:c.-182C= ENSP00000504262.1:n.-182C=
ENST00000260118.6:c.-182C= ENSP00000260118.6:n.-182C=
NM_003878.2:c.-182C= NP_003869.1:n.-182C=
XM_011517623.1:c.-182C= XP_011515925.1:n.-182C=