Canonical Allele Identifier: CA2732014312
Gene: SCNN1G HGNC NCBI

Linked Data

dbSNP Id: rs2141944273

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23211375G>A , CM000678.2:g.23211375G>A GRCh38
NC_000016.9:g.23222696G>A , CM000678.1:g.23222696G>A GRCh37
NC_000016.8:g.23130197G>A NCBI36
NG_011909.1:g.33657G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.1177-659G>A MANE Select ENSP00000300061.2:n.1177-659G>A
ENST00000300061.2:c.1177-659G>A ENSP00000300061.2:n.1177-659G>A
NM_001039.3:c.1177-659G>A NP_001030.2:n.1177-659G>A
NM_001039.4:c.1177-659G>A MANE Select NP_001030.2:n.1177-659G>A