Canonical Allele Identifier: CA975705338
Gene: SCNN1G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23196722C>A , CM000678.2:g.23196722C>A GRCh38
NC_000016.9:g.23208043C>A , CM000678.1:g.23208043C>A GRCh37
NC_000016.8:g.23115544C>A NCBI36
NG_011909.1:g.19004C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.914-542C>A MANE Select ENSP00000300061.2:n.914-542C>A
ENST00000300061.2:c.914-542C>A ENSP00000300061.2:n.914-542C>A
NM_001039.3:c.914-542C>A NP_001030.2:n.914-542C>A
NM_001039.4:c.914-542C>A MANE Select NP_001030.2:n.914-542C>A