Canonical Allele Identifier: CA2213232967
Gene: SCNN1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23211371C= , CM000678.2:g.23211371C= GRCh38
NC_000016.9:g.23222692C= , CM000678.1:g.23222692C= GRCh37
NC_000016.8:g.23130193C= NCBI36
NG_011909.1:g.33653C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.1177-663C= MANE Select ENSP00000300061.2:n.1177-663C=
ENST00000300061.2:c.1177-663C= ENSP00000300061.2:n.1177-663C=
NM_001039.3:c.1177-663C= NP_001030.2:n.1177-663C=
NM_001039.4:c.1177-663C= MANE Select NP_001030.2:n.1177-663C=