Canonical Allele Identifier: CA854142236
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs1306327682
MyVariant Identifiers: chr8:g.63951396C>G (hg19) chr8:g.63038837C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038837C>G , CM000670.2:g.63038837C>G GRCh38
NC_000008.10:g.63951396C>G , CM000670.1:g.63951396C>G GRCh37
NC_000008.9:g.64113950C>G NCBI36
NG_028126.1:g.5215G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.571G>C
ENST00000677482.1:c.-69G>C ENSP00000504590.1:n.-69G>C
ENST00000679326.1:c.-69G>C ENSP00000504262.1:n.-69G>C
ENST00000260118.6:c.-69G>C ENSP00000260118.6:n.-69G>C
NM_003878.2:c.-69G>C NP_003869.1:n.-69G>C
XM_011517623.1:c.-69G>C XP_011515925.1:n.-69G>C
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