Canonical Allele Identifier: CA178367041
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs549910927
gnomAD v3: 8-63038993-C-A
gnomAD v4: 8-63038993-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038993C>A , CM000670.2:g.63038993C>A GRCh38
NC_000008.10:g.63951552C>A , CM000670.1:g.63951552C>A GRCh37
NC_000008.9:g.64114106C>A NCBI36
NG_028126.1:g.5059G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.415G>T
ENST00000679326.1:c.-225G>T ENSP00000504262.1:n.-225G>T
ENST00000260118.6:c.-225G>T ENSP00000260118.6:n.-225G>T
NM_003878.2:c.-225G>T NP_003869.1:n.-225G>T
XM_011517623.1:c.-225G>T XP_011515925.1:n.-225G>T