Canonical Allele Identifier: CA9026147
Gene: ELANE HGNC NCBI

Linked Data

ClinVar Variation Id: 668759
ClinVar RCV Id: RCV000827715 RCV001796261
dbSNP Id: rs202059602
ExAC: 19:856062 G / A
gnomAD v2: 19-856062-G-A
gnomAD v3: 19-856062-G-A
gnomAD v4: 19-856062-G-A
MyVariant Identifiers: chr19:g.856062G>A (hg19) chr19:g.856062G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.856062G>A , CM000681.2:g.856062G>A GRCh38
NC_000019.9:g.856062G>A , CM000681.1:g.856062G>A GRCh37
NC_000019.8:g.807062G>A NCBI36
NG_007274.1:g.1398G>A , LRG_46:g.1398G>A
NG_009627.1:g.8772G>A , LRG_57:g.8772G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.702G>A MANE Select ENSP00000263621.1:p.Pro234=
ENST00000263621.1:c.702G>A ENSP00000263621.1:p.Pro234=
ENST00000590230.5:c.702G>A ENSP00000466090.1:p.Pro234=
NM_001972.2:c.702G>A , LRG_57t1:c.702G>A NP_001963.1:p.Pro234=
XM_011527775.1:c.702G>A XP_011526077.1:p.Pro234=
XM_011527776.1:c.702G>A XP_011526078.1:p.Pro234=
NM_001972.3:c.702G>A NP_001963.1:p.Pro234=
NM_001972.4:c.702G>A MANE Select NP_001963.1:p.Pro234=
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