Canonical Allele Identifier: CA666003795

Gene: DRGX

Linked Data

• dbSNP Id: rs1234849361
• gnomAD v3: 10-49368638-T-C
• gnomAD v4: 10-49368638-T-C
• MyVariant Identifiers: chr10:g.50576683T>C (hg19) ; chr10:g.49368638T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49368638T>C , CM000672.2:g.49368638T>C	GRCh38
NC_000010.10:g.50576683T>C , CM000672.1:g.50576683T>C	GRCh37
NC_000010.9:g.50246689T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000374139.8:c.527-2257A>G MANE Select	ENSP00000363254.1:n.527-2257A>G
ENST00000374139.6:c.527-2257A>G	ENSP00000363254.1:n.527-2257A>G
ENST00000434016.2:c.527-2257A>G	ENSP00000401653.2:n.527-2257A>G
NM_001276451.1:c.527-2257A>G	NP_001263380.1:n.527-2257A>G
XM_011540089.1:c.632-2257A>G	XP_011538391.1:n.632-2257A>G
XM_011540090.1:c.212-2257A>G	XP_011538392.1:n.212-2257A>G
XM_011540089.3:c.632-2257A>G	XP_011538391.1:n.632-2257A>G
NM_001276451.2:c.527-2257A>G MANE Select	NP_001263380.1:n.527-2257A>G