Canonical Allele Identifier: CA975678177
Gene: SCNN1G HGNC NCBI

Linked Data

dbSNP Id: rs1960076730

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23211393_23211394del , CM000678.2:g.23211393_23211394del GRCh38
NC_000016.9:g.23222714_23222715del , CM000678.1:g.23222714_23222715del GRCh37
NC_000016.8:g.23130215_23130216del NCBI36
NG_011909.1:g.33675_33676del

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.1177-641_1177-640del MANE Select ENSP00000300061.2:n.1177-641_1177-640del
ENST00000300061.2:c.1177-641_1177-640del ENSP00000300061.2:n.1177-641_1177-640del
NM_001039.3:c.1177-641_1177-640del NP_001030.2:n.1177-641_1177-640del
NM_001039.4:c.1177-641_1177-640del MANE Select NP_001030.2:n.1177-641_1177-640del