Canonical Allele Identifier: CA1788923467
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs1804968664
gnomAD v4: 8-63038905-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038905T>G , CM000670.2:g.63038905T>G GRCh38
NC_000008.10:g.63951464T>G , CM000670.1:g.63951464T>G GRCh37
NC_000008.9:g.64114018T>G NCBI36
NG_028126.1:g.5147A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.503A>C
ENST00000679326.1:c.-137A>C ENSP00000504262.1:n.-137A>C
ENST00000260118.6:c.-137A>C ENSP00000260118.6:n.-137A>C
NM_003878.2:c.-137A>C NP_003869.1:n.-137A>C
XM_011517623.1:c.-137A>C XP_011515925.1:n.-137A>C
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