Canonical Allele Identifier: CA227938
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 99829
ClinVar RCV Id: RCV000086262
dbSNP Id: rs62637038
gnomAD v4: X-41474562-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474562G>T , CM000685.2:g.41474562G>T GRCh38
NC_000023.10:g.41333815G>T , CM000685.1:g.41333815G>T GRCh37
NC_000023.9:g.41218759G>T NCBI36
NG_009112.1:g.32103G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1094G>T ENSP00000340328.3:p.Gly365Val
ENST00000378220.3:c.1094G>T MANE Select ENSP00000367465.2:p.Gly365Val
ENST00000378220.2:c.1109G>T ENSP00000367465.1:p.Gly370Val
ENST00000342595.2:c.1109G>T ENSP00000340328.2:p.Gly370Val
ENST00000378220.1:c.1109G>T ENSP00000367465.1:p.Gly370Val
NM_022567.2:c.1109G>T NP_072089.1:p.Gly370Val
XM_005272632.2:c.1109G>T XP_005272689.1:p.Gly370Val
XM_017029709.1:c.1109G>T XP_016885198.1:p.Gly370Val
NM_001378477.3:c.1094G>T MANE Select NP_001365406.2:p.Gly365Val
NM_022567.3:c.1094G>T NP_072089.2:p.Gly365Val