Canonical Allele Identifier: CA2599392807
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs2129694276
gnomAD v3: 8-63038938-G-C
gnomAD v4: 8-63038938-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038938G>C , CM000670.2:g.63038938G>C GRCh38
NC_000008.10:g.63951497G>C , CM000670.1:g.63951497G>C GRCh37
NC_000008.9:g.64114051G>C NCBI36
NG_028126.1:g.5114C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.470C>G
ENST00000679326.1:c.-170C>G ENSP00000504262.1:n.-170C>G
ENST00000260118.6:c.-170C>G ENSP00000260118.6:n.-170C>G
NM_003878.2:c.-170C>G NP_003869.1:n.-170C>G
XM_011517623.1:c.-170C>G XP_011515925.1:n.-170C>G