Canonical Allele Identifier: CA178366944
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs4590435
gnomAD v4: 8-63038924-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038924G>A , CM000670.2:g.63038924G>A GRCh38
NC_000008.10:g.63951483G>A , CM000670.1:g.63951483G>A GRCh37
NC_000008.9:g.64114037G>A NCBI36
NG_028126.1:g.5128C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.484C>T
ENST00000679326.1:c.-156C>T ENSP00000504262.1:n.-156C>T
ENST00000260118.6:c.-156C>T ENSP00000260118.6:n.-156C>T
NM_003878.2:c.-156C>T NP_003869.1:n.-156C>T
XM_011517623.1:c.-156C>T XP_011515925.1:n.-156C>T