Canonical Allele Identifier: CA2632290401
Gene: SCNN1G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23196648A>G , CM000678.2:g.23196648A>G GRCh38
NC_000016.9:g.23207969A>G , CM000678.1:g.23207969A>G GRCh37
NC_000016.8:g.23115470A>G NCBI36
NG_011909.1:g.18930A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300061.3:c.914-616A>G MANE Select ENSP00000300061.2:n.914-616A>G
ENST00000300061.2:c.914-616A>G ENSP00000300061.2:n.914-616A>G
NM_001039.3:c.914-616A>G NP_001030.2:n.914-616A>G
NM_001039.4:c.914-616A>G MANE Select NP_001030.2:n.914-616A>G