Canonical Allele Identifier: CA2213232905
Gene: SCNN1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23211257C= , CM000678.2:g.23211257C= GRCh38
NC_000016.9:g.23222578C= , CM000678.1:g.23222578C= GRCh37
NC_000016.8:g.23130079C= NCBI36
NG_011909.1:g.33539C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.1177-777C= MANE Select ENSP00000300061.2:n.1177-777C=
ENST00000300061.2:c.1177-777C= ENSP00000300061.2:n.1177-777C=
NM_001039.3:c.1177-777C= NP_001030.2:n.1177-777C=
NM_001039.4:c.1177-777C= MANE Select NP_001030.2:n.1177-777C=