Canonical Allele Identifier: CA854142197
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs1325813210
MyVariant Identifiers: chr8:g.63951364del (hg19) chr8:g.63038805del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038805del , CM000670.2:g.63038805del GRCh38
NC_000008.10:g.63951364del , CM000670.1:g.63951364del GRCh37
NC_000008.9:g.64113918del NCBI36
NG_028126.1:g.5247del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260118.7:c.-37del MANE Select ENSP00000260118.6:n.-37del
ENST00000677327.1:n.603del
ENST00000677482.1:c.-37del ENSP00000504590.1:n.-37del
ENST00000679326.1:c.-37del ENSP00000504262.1:n.-37del
ENST00000260118.6:c.-37del ENSP00000260118.6:n.-37del
NM_003878.2:c.-37del NP_003869.1:n.-37del
XM_011517623.1:c.-37del XP_011515925.1:n.-37del
NM_003878.3:c.-37del MANE Select NP_003869.1:n.-37del
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