Canonical Allele Identifier: CA1788923604
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs1489471824
gnomAD v4: 8-63039086-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039086G>A , CM000670.2:g.63039086G>A GRCh38
NC_000008.10:g.63951645G>A , CM000670.1:g.63951645G>A GRCh37
NC_000008.9:g.64114199G>A NCBI36
NG_028126.1:g.4966C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.322C>T
ENST00000679326.1:c.-318C>T ENSP00000504262.1:n.-318C>T
ENST00000260118.6:c.-318C>T ENSP00000260118.6:n.-318C>T
XM_011517623.1:c.-318C>T XP_011515925.1:n.-318C>T