Canonical Allele Identifier: CA2213223819
Gene: SCNN1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23196623T= , CM000678.2:g.23196623T= GRCh38
NC_000016.9:g.23207944T= , CM000678.1:g.23207944T= GRCh37
NC_000016.8:g.23115445T= NCBI36
NG_011909.1:g.18905T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300061.3:c.914-641T= MANE Select ENSP00000300061.2:n.914-641T=
ENST00000300061.2:c.914-641T= ENSP00000300061.2:n.914-641T=
NM_001039.3:c.914-641T= NP_001030.2:n.914-641T=
NM_001039.4:c.914-641T= MANE Select NP_001030.2:n.914-641T=