Canonical Allele Identifier: CA1788923592
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs1585677448
gnomAD v4: 8-63039074-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039074G>C , CM000670.2:g.63039074G>C GRCh38
NC_000008.10:g.63951633G>C , CM000670.1:g.63951633G>C GRCh37
NC_000008.9:g.64114187G>C NCBI36
NG_028126.1:g.4978C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.334C>G
ENST00000679326.1:c.-306C>G ENSP00000504262.1:n.-306C>G
ENST00000260118.6:c.-306C>G ENSP00000260118.6:n.-306C>G
XM_011517623.1:c.-306C>G XP_011515925.1:n.-306C>G