Canonical Allele Identifier: CA279450285
Gene: SCNN1G HGNC NCBI

Linked Data

dbSNP Id: rs943451302

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23196730C>T , CM000678.2:g.23196730C>T GRCh38
NC_000016.9:g.23208051C>T , CM000678.1:g.23208051C>T GRCh37
NC_000016.8:g.23115552C>T NCBI36
NG_011909.1:g.19012C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.914-534C>T MANE Select ENSP00000300061.2:n.914-534C>T
ENST00000300061.2:c.914-534C>T ENSP00000300061.2:n.914-534C>T
NM_001039.3:c.914-534C>T NP_001030.2:n.914-534C>T
NM_001039.4:c.914-534C>T MANE Select NP_001030.2:n.914-534C>T