Canonical Allele Identifier: CA10389910
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 2097700
ClinVar RCV Id: RCV003018936
dbSNP Id: rs768139938
ExAC: X:41333845 G / A
gnomAD v2: X-41333845-G-A
gnomAD v3: X-41474592-G-A
gnomAD v4: X-41474592-G-A
MyVariant Identifiers: chrX:g.41333845G>A (hg19) chrX:g.41474592G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474592G>A , CM000685.2:g.41474592G>A GRCh38
NC_000023.10:g.41333845G>A , CM000685.1:g.41333845G>A GRCh37
NC_000023.9:g.41218789G>A NCBI36
NG_009112.1:g.32133G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1124G>A ENSP00000340328.3:p.Arg375His
ENST00000378220.3:c.1124G>A MANE Select ENSP00000367465.2:p.Arg375His
ENST00000378220.2:c.1139G>A ENSP00000367465.1:p.Arg380His
ENST00000342595.2:c.1139G>A ENSP00000340328.2:p.Arg380His
ENST00000378220.1:c.1139G>A ENSP00000367465.1:p.Arg380His
NM_022567.2:c.1139G>A NP_072089.1:p.Arg380His
XM_005272632.2:c.1139G>A XP_005272689.1:p.Arg380His
XM_017029709.1:c.1139G>A XP_016885198.1:p.Arg380His
NM_001378477.3:c.1124G>A MANE Select NP_001365406.2:p.Arg375His
NM_022567.3:c.1124G>A NP_072089.2:p.Arg375His
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