Canonical Allele Identifier: CA504686609
Gene: ELANE HGNC NCBI

Linked Data

dbSNP Id: rs750556860
MyVariant Identifiers: chr19:g.856020G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.856020G>A , CM000681.2:g.856020G>A GRCh38
NC_000019.9:g.856020G>A , CM000681.1:g.856020G>A GRCh37
NC_000019.8:g.807020G>A NCBI36
NG_007274.1:g.1356G>A , LRG_46:g.1356G>A
NG_009627.1:g.8730G>A , LRG_57:g.8730G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263621.2:c.660G>A MANE Select ENSP00000263621.1:p.Arg220=
ENST00000263621.1:c.660G>A ENSP00000263621.1:p.Arg220=
ENST00000590230.5:c.660G>A ENSP00000466090.1:p.Arg220=
NM_001972.2:c.660G>A , LRG_57t1:c.660G>A NP_001963.1:p.Arg220=
XM_011527775.1:c.660G>A XP_011526077.1:p.Arg220=
XM_011527776.1:c.660G>A XP_011526078.1:p.Arg220=
NM_001972.3:c.660G>A NP_001963.1:p.Arg220=
NM_001972.4:c.660G>A MANE Select NP_001963.1:p.Arg220=