Canonical Allele Identifier: CA2213223874

Gene: SCNN1G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23196758G= , CM000678.2:g.23196758G=	GRCh38
NC_000016.9:g.23208079G= , CM000678.1:g.23208079G=	GRCh37
NC_000016.8:g.23115580G=	NCBI36
NG_011909.1:g.19040G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300061.3:c.914-506G= MANE Select	ENSP00000300061.2:n.914-506G=
ENST00000300061.2:c.914-506G=	ENSP00000300061.2:n.914-506G=
NM_001039.3:c.914-506G=	NP_001030.2:n.914-506G=
NM_001039.4:c.914-506G= MANE Select	NP_001030.2:n.914-506G=