Canonical Allele Identifier: CA1788923448
Gene: GGH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038867G= , CM000670.2:g.63038867G= GRCh38
NC_000008.10:g.63951426G= , CM000670.1:g.63951426G= GRCh37
NC_000008.9:g.64113980G= NCBI36
NG_028126.1:g.5185C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.541C=
ENST00000677482.1:c.-99C= ENSP00000504590.1:n.-99C=
ENST00000679326.1:c.-99C= ENSP00000504262.1:n.-99C=
ENST00000260118.6:c.-99C= ENSP00000260118.6:n.-99C=
NM_003878.2:c.-99C= NP_003869.1:n.-99C=
XM_011517623.1:c.-99C= XP_011515925.1:n.-99C=
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