Canonical Allele Identifier: CA504684737
Gene: ELANE HGNC NCBI

Linked Data

gnomAD v4: 19-852964-C-T
MyVariant Identifiers: chr19:g.852964C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.852964C>T , CM000681.2:g.852964C>T GRCh38
NC_000019.9:g.852964C>T , CM000681.1:g.852964C>T GRCh37
NC_000019.8:g.803964C>T NCBI36
NG_009627.1:g.5674C>T , LRG_57:g.5674C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263621.2:c.156C>T MANE Select ENSP00000263621.1:p.Gly52=
ENST00000263621.1:c.156C>T ENSP00000263621.1:p.Gly52=
ENST00000590230.5:c.156C>T ENSP00000466090.1:p.Gly52=
NM_001972.2:c.156C>T , LRG_57t1:c.156C>T NP_001963.1:p.Gly52=
XM_011527775.1:c.156C>T XP_011526077.1:p.Gly52=
XM_011527776.1:c.156C>T XP_011526078.1:p.Gly52=
NM_001972.3:c.156C>T NP_001963.1:p.Gly52=
NM_001972.4:c.156C>T MANE Select NP_001963.1:p.Gly52=