Canonical Allele Identifier: CA2687440328
Gene: GGH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039073_63039074insA , CM000670.2:g.63039073_63039074insA GRCh38
NC_000008.10:g.63951632_63951633insA , CM000670.1:g.63951632_63951633insA GRCh37
NC_000008.9:g.64114186_64114187insA NCBI36
NG_028126.1:g.4978_4979insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.334_335insT
ENST00000679326.1:c.-306_-305insT ENSP00000504262.1:n.-306_-305insT
ENST00000260118.6:c.-306_-305insT ENSP00000260118.6:n.-306_-305insT
XM_011517623.1:c.-306_-305insT XP_011515925.1:n.-306_-305insT