Canonical Allele Identifier: CA2213232965
Gene: SCNN1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23211367A= , CM000678.2:g.23211367A= GRCh38
NC_000016.9:g.23222688A= , CM000678.1:g.23222688A= GRCh37
NC_000016.8:g.23130189A= NCBI36
NG_011909.1:g.33649A=

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.1177-667A= MANE Select ENSP00000300061.2:n.1177-667A=
ENST00000300061.2:c.1177-667A= ENSP00000300061.2:n.1177-667A=
NM_001039.3:c.1177-667A= NP_001030.2:n.1177-667A=
NM_001039.4:c.1177-667A= MANE Select NP_001030.2:n.1177-667A=