Canonical Allele Identifier: CA1788923470
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs901278772

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038916_63038917dup , CM000670.2:g.63038916_63038917dup GRCh38
NC_000008.10:g.63951475_63951476dup , CM000670.1:g.63951475_63951476dup GRCh37
NC_000008.9:g.64114029_64114030dup NCBI36
NG_028126.1:g.5141_5142dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.497_498dup
ENST00000679326.1:c.-143_-142dup ENSP00000504262.1:n.-143_-142dup
ENST00000260118.6:c.-143_-142dup ENSP00000260118.6:n.-143_-142dup
NM_003878.2:c.-143_-142dup NP_003869.1:n.-143_-142dup
XM_011517623.1:c.-143_-142dup XP_011515925.1:n.-143_-142dup