Canonical Allele Identifier: CA1788923386
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038809G= , CM000670.2:g.63038809G= GRCh38
NC_000008.10:g.63951368G= , CM000670.1:g.63951368G= GRCh37
NC_000008.9:g.64113922G= NCBI36
NG_028126.1:g.5243C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.599C=
ENST00000677482.1:c.-41C= ENSP00000504590.1:n.-41C=
ENST00000679326.1:c.-41C= ENSP00000504262.1:n.-41C=
ENST00000260118.6:c.-41C= ENSP00000260118.6:n.-41C=
NM_003878.2:c.-41C= NP_003869.1:n.-41C=
XM_011517623.1:c.-41C= XP_011515925.1:n.-41C=