Canonical Allele Identifier: CA2213223823
Gene: SCNN1G HGNC NCBI

Linked Data

dbSNP Id: rs1959798885

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23196630G>A , CM000678.2:g.23196630G>A GRCh38
NC_000016.9:g.23207951G>A , CM000678.1:g.23207951G>A GRCh37
NC_000016.8:g.23115452G>A NCBI36
NG_011909.1:g.18912G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300061.3:c.914-634G>A MANE Select ENSP00000300061.2:n.914-634G>A
ENST00000300061.2:c.914-634G>A ENSP00000300061.2:n.914-634G>A
NM_001039.3:c.914-634G>A NP_001030.2:n.914-634G>A
NM_001039.4:c.914-634G>A MANE Select NP_001030.2:n.914-634G>A