Canonical Allele Identifier: CA2213233000
Gene: SCNN1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23211409C= , CM000678.2:g.23211409C= GRCh38
NC_000016.9:g.23222730C= , CM000678.1:g.23222730C= GRCh37
NC_000016.8:g.23130231C= NCBI36
NG_011909.1:g.33691C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.1177-625C= MANE Select ENSP00000300061.2:n.1177-625C=
ENST00000300061.2:c.1177-625C= ENSP00000300061.2:n.1177-625C=
NM_001039.3:c.1177-625C= NP_001030.2:n.1177-625C=
NM_001039.4:c.1177-625C= MANE Select NP_001030.2:n.1177-625C=