Canonical Allele Identifier: CA1788923587
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs1585677437

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039069T>A , CM000670.2:g.63039069T>A GRCh38
NC_000008.10:g.63951628T>A , CM000670.1:g.63951628T>A GRCh37
NC_000008.9:g.64114182T>A NCBI36
NG_028126.1:g.4983A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.339A>T
ENST00000679326.1:c.-301A>T ENSP00000504262.1:n.-301A>T
ENST00000260118.6:c.-301A>T ENSP00000260118.6:n.-301A>T
XM_011517623.1:c.-301A>T XP_011515925.1:n.-301A>T