Canonical Allele Identifier: CA2687440385
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs2129695052
gnomAD v4: 8-63039111-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039111G>A , CM000670.2:g.63039111G>A GRCh38
NC_000008.10:g.63951670G>A , CM000670.1:g.63951670G>A GRCh37
NC_000008.9:g.64114224G>A NCBI36
NG_028126.1:g.4941C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.297C>T
ENST00000679326.1:c.-343C>T ENSP00000504262.1:n.-343C>T
ENST00000260118.6:c.-343C>T ENSP00000260118.6:n.-343C>T
XM_011517623.1:c.-343C>T XP_011515925.1:n.-343C>T