Canonical Allele Identifier: CA1788923511
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs1804970151

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038958A>C , CM000670.2:g.63038958A>C GRCh38
NC_000008.10:g.63951517A>C , CM000670.1:g.63951517A>C GRCh37
NC_000008.9:g.64114071A>C NCBI36
NG_028126.1:g.5094T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.450T>G
ENST00000679326.1:c.-190T>G ENSP00000504262.1:n.-190T>G
ENST00000260118.6:c.-190T>G ENSP00000260118.6:n.-190T>G
NM_003878.2:c.-190T>G NP_003869.1:n.-190T>G
XM_011517623.1:c.-190T>G XP_011515925.1:n.-190T>G