Canonical Allele Identifier: CA1908701568
Gene: DRGX HGNC NCBI

Linked Data

dbSNP Id: rs1849623768
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49368617C>T , CM000672.2:g.49368617C>T GRCh38
NC_000010.10:g.50576662C>T , CM000672.1:g.50576662C>T GRCh37
NC_000010.9:g.50246668C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374139.8:c.527-2236G>A MANE Select ENSP00000363254.1:n.527-2236G>A
ENST00000374139.6:c.527-2236G>A ENSP00000363254.1:n.527-2236G>A
ENST00000434016.2:c.527-2236G>A ENSP00000401653.2:n.527-2236G>A
NM_001276451.1:c.527-2236G>A NP_001263380.1:n.527-2236G>A
XM_011540089.1:c.632-2236G>A XP_011538391.1:n.632-2236G>A
XM_011540090.1:c.212-2236G>A XP_011538392.1:n.212-2236G>A
XM_011540089.3:c.632-2236G>A XP_011538391.1:n.632-2236G>A
NM_001276451.2:c.527-2236G>A MANE Select NP_001263380.1:n.527-2236G>A
Search 100 bp 5'
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