Canonical Allele Identifier: CA2213223919
Gene: SCNN1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23196859T= , CM000678.2:g.23196859T= GRCh38
NC_000016.9:g.23208180T= , CM000678.1:g.23208180T= GRCh37
NC_000016.8:g.23115681T= NCBI36
NG_011909.1:g.19141T=

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.914-405T= MANE Select ENSP00000300061.2:n.914-405T=
ENST00000300061.2:c.914-405T= ENSP00000300061.2:n.914-405T=
NM_001039.3:c.914-405T= NP_001030.2:n.914-405T=
NM_001039.4:c.914-405T= MANE Select NP_001030.2:n.914-405T=