Canonical Allele Identifier: CA1114587687
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs1804974094
gnomAD v3: 8-63039114-G-A
gnomAD v4: 8-63039114-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039114G>A , CM000670.2:g.63039114G>A GRCh38
NC_000008.10:g.63951673G>A , CM000670.1:g.63951673G>A GRCh37
NC_000008.9:g.64114227G>A NCBI36
NG_028126.1:g.4938C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.294C>T
ENST00000679326.1:c.-346C>T ENSP00000504262.1:n.-346C>T
ENST00000260118.6:c.-346C>T ENSP00000260118.6:n.-346C>T
XM_011517623.1:c.-346C>T XP_011515925.1:n.-346C>T