Canonical Allele Identifier: CA14215991
Gene: SCNN1G HGNC NCBI

Linked Data

dbSNP Id: rs13331086

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23196796T>G , CM000678.2:g.23196796T>G GRCh38
NC_000016.9:g.23208117T>G , CM000678.1:g.23208117T>G GRCh37
NC_000016.8:g.23115618T>G NCBI36
NG_011909.1:g.19078T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.914-468T>G MANE Select ENSP00000300061.2:n.914-468T>G
ENST00000300061.2:c.914-468T>G ENSP00000300061.2:n.914-468T>G
NM_001039.3:c.914-468T>G NP_001030.2:n.914-468T>G
NM_001039.4:c.914-468T>G MANE Select NP_001030.2:n.914-468T>G