Canonical Allele Identifier: CA719190227
Gene: SCNN1G HGNC NCBI

Linked Data

dbSNP Id: rs1239316081

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23196846del , CM000678.2:g.23196846del GRCh38
NC_000016.9:g.23208167del , CM000678.1:g.23208167del GRCh37
NC_000016.8:g.23115668del NCBI36
NG_011909.1:g.19128del

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.914-418del MANE Select ENSP00000300061.2:n.914-418del
ENST00000300061.2:c.914-418del ENSP00000300061.2:n.914-418del
NM_001039.3:c.914-418del NP_001030.2:n.914-418del
NM_001039.4:c.914-418del MANE Select NP_001030.2:n.914-418del