Canonical Allele Identifier: CA206600056
Gene: DRGX HGNC NCBI

Linked Data

dbSNP Id: rs993826401
MyVariant Identifiers: chr10:g.50576656A>G (hg19) chr10:g.49368611A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49368611A>G , CM000672.2:g.49368611A>G GRCh38
NC_000010.10:g.50576656A>G , CM000672.1:g.50576656A>G GRCh37
NC_000010.9:g.50246662A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374139.8:c.527-2230T>C MANE Select ENSP00000363254.1:n.527-2230T>C
ENST00000374139.6:c.527-2230T>C ENSP00000363254.1:n.527-2230T>C
ENST00000434016.2:c.527-2230T>C ENSP00000401653.2:n.527-2230T>C
NM_001276451.1:c.527-2230T>C NP_001263380.1:n.527-2230T>C
XM_011540089.1:c.632-2230T>C XP_011538391.1:n.632-2230T>C
XM_011540090.1:c.212-2230T>C XP_011538392.1:n.212-2230T>C
XM_011540089.3:c.632-2230T>C XP_011538391.1:n.632-2230T>C
NM_001276451.2:c.527-2230T>C MANE Select NP_001263380.1:n.527-2230T>C
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