Canonical Allele Identifier: CA2213223807

Gene: SCNN1G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23196606G= , CM000678.2:g.23196606G=	GRCh38
NC_000016.9:g.23207927G= , CM000678.1:g.23207927G=	GRCh37
NC_000016.8:g.23115428G=	NCBI36
NG_011909.1:g.18888G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300061.3:c.914-658G= MANE Select	ENSP00000300061.2:n.914-658G=
ENST00000300061.2:c.914-658G=	ENSP00000300061.2:n.914-658G=
NM_001039.3:c.914-658G=	NP_001030.2:n.914-658G=
NM_001039.4:c.914-658G= MANE Select	NP_001030.2:n.914-658G=