Canonical Allele Identifier: CA2717289055
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs2129694318
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038944G>T , CM000670.2:g.63038944G>T GRCh38
NC_000008.10:g.63951503G>T , CM000670.1:g.63951503G>T GRCh37
NC_000008.9:g.64114057G>T NCBI36
NG_028126.1:g.5108C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.464C>A
ENST00000679326.1:c.-176C>A ENSP00000504262.1:n.-176C>A
ENST00000260118.6:c.-176C>A ENSP00000260118.6:n.-176C>A
NM_003878.2:c.-176C>A NP_003869.1:n.-176C>A
XM_011517623.1:c.-176C>A XP_011515925.1:n.-176C>A
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