Canonical Allele Identifier: CA2780586671
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038942G>A , CM000670.2:g.63038942G>A GRCh38
NC_000008.10:g.63951501G>A , CM000670.1:g.63951501G>A GRCh37
NC_000008.9:g.64114055G>A NCBI36
NG_028126.1:g.5110C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.466C>T
ENST00000679326.1:c.-174C>T ENSP00000504262.1:n.-174C>T
ENST00000260118.6:c.-174C>T ENSP00000260118.6:n.-174C>T
NM_003878.2:c.-174C>T NP_003869.1:n.-174C>T
XM_011517623.1:c.-174C>T XP_011515925.1:n.-174C>T