Canonical Allele Identifier: CA1788923487
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs1804969352
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038933C>A , CM000670.2:g.63038933C>A GRCh38
NC_000008.10:g.63951492C>A , CM000670.1:g.63951492C>A GRCh37
NC_000008.9:g.64114046C>A NCBI36
NG_028126.1:g.5119G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.475G>T
ENST00000679326.1:c.-165G>T ENSP00000504262.1:n.-165G>T
ENST00000260118.6:c.-165G>T ENSP00000260118.6:n.-165G>T
NM_003878.2:c.-165G>T NP_003869.1:n.-165G>T
XM_011517623.1:c.-165G>T XP_011515925.1:n.-165G>T
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