Canonical Allele Identifier: CA854142383
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs1299630994
gnomAD v3: 8-63039024-C-T
gnomAD v4: 8-63039024-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039024C>T , CM000670.2:g.63039024C>T GRCh38
NC_000008.10:g.63951583C>T , CM000670.1:g.63951583C>T GRCh37
NC_000008.9:g.64114137C>T NCBI36
NG_028126.1:g.5028G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.384G>A
ENST00000679326.1:c.-256G>A ENSP00000504262.1:n.-256G>A
ENST00000260118.6:c.-256G>A ENSP00000260118.6:n.-256G>A
NM_003878.2:c.-256G>A NP_003869.1:n.-256G>A
XM_011517623.1:c.-256G>A XP_011515925.1:n.-256G>A