Canonical Allele Identifier: CA2213223855
Gene: SCNN1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23196725T= , CM000678.2:g.23196725T= GRCh38
NC_000016.9:g.23208046T= , CM000678.1:g.23208046T= GRCh37
NC_000016.8:g.23115547T= NCBI36
NG_011909.1:g.19007T=

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.914-539T= MANE Select ENSP00000300061.2:n.914-539T=
ENST00000300061.2:c.914-539T= ENSP00000300061.2:n.914-539T=
NM_001039.3:c.914-539T= NP_001030.2:n.914-539T=
NM_001039.4:c.914-539T= MANE Select NP_001030.2:n.914-539T=