Canonical Allele Identifier: CA504686408
Gene: ELANE HGNC NCBI

Linked Data

dbSNP Id: rs2035674043
gnomAD v3: 19-855981-C-G
gnomAD v4: 19-855981-C-G
MyVariant Identifiers: chr19:g.855981C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.855981C>G , CM000681.2:g.855981C>G GRCh38
NC_000019.9:g.855981C>G , CM000681.1:g.855981C>G GRCh37
NC_000019.8:g.806981C>G NCBI36
NG_007274.1:g.1317C>G , LRG_46:g.1317C>G
NG_009627.1:g.8691C>G , LRG_57:g.8691C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263621.2:c.621C>G MANE Select ENSP00000263621.1:p.Val207=
ENST00000263621.1:c.621C>G ENSP00000263621.1:p.Val207=
ENST00000590230.5:c.621C>G ENSP00000466090.1:p.Val207=
NM_001972.2:c.621C>G , LRG_57t1:c.621C>G NP_001963.1:p.Val207=
XM_011527775.1:c.621C>G XP_011526077.1:p.Val207=
XM_011527776.1:c.621C>G XP_011526078.1:p.Val207=
NM_001972.3:c.621C>G NP_001963.1:p.Val207=
NM_001972.4:c.621C>G MANE Select NP_001963.1:p.Val207=