Canonical Allele Identifier: CA2213223815
Gene: SCNN1G HGNC NCBI

Linked Data

dbSNP Id: rs1959798700

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23196615T>A , CM000678.2:g.23196615T>A GRCh38
NC_000016.9:g.23207936T>A , CM000678.1:g.23207936T>A GRCh37
NC_000016.8:g.23115437T>A NCBI36
NG_011909.1:g.18897T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300061.3:c.914-649T>A MANE Select ENSP00000300061.2:n.914-649T>A
ENST00000300061.2:c.914-649T>A ENSP00000300061.2:n.914-649T>A
NM_001039.3:c.914-649T>A NP_001030.2:n.914-649T>A
NM_001039.4:c.914-649T>A MANE Select NP_001030.2:n.914-649T>A