Canonical Allele Identifier: CA2213232986
Gene: SCNN1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23211391C= , CM000678.2:g.23211391C= GRCh38
NC_000016.9:g.23222712C= , CM000678.1:g.23222712C= GRCh37
NC_000016.8:g.23130213C= NCBI36
NG_011909.1:g.33673C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.1177-643C= MANE Select ENSP00000300061.2:n.1177-643C=
ENST00000300061.2:c.1177-643C= ENSP00000300061.2:n.1177-643C=
NM_001039.3:c.1177-643C= NP_001030.2:n.1177-643C=
NM_001039.4:c.1177-643C= MANE Select NP_001030.2:n.1177-643C=