Canonical Allele Identifier: CA2717288694
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs2129693943
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038859A>G , CM000670.2:g.63038859A>G GRCh38
NC_000008.10:g.63951418A>G , CM000670.1:g.63951418A>G GRCh37
NC_000008.9:g.64113972A>G NCBI36
NG_028126.1:g.5193T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.549T>C
ENST00000677482.1:c.-91T>C ENSP00000504590.1:n.-91T>C
ENST00000679326.1:c.-91T>C ENSP00000504262.1:n.-91T>C
ENST00000260118.6:c.-91T>C ENSP00000260118.6:n.-91T>C
NM_003878.2:c.-91T>C NP_003869.1:n.-91T>C
XM_011517623.1:c.-91T>C XP_011515925.1:n.-91T>C
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