Canonical Allele Identifier: CA2213232917
Gene: SCNN1G HGNC NCBI

Linked Data

dbSNP Id: rs1960075090

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23211274T>C , CM000678.2:g.23211274T>C GRCh38
NC_000016.9:g.23222595T>C , CM000678.1:g.23222595T>C GRCh37
NC_000016.8:g.23130096T>C NCBI36
NG_011909.1:g.33556T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.1177-760T>C MANE Select ENSP00000300061.2:n.1177-760T>C
ENST00000300061.2:c.1177-760T>C ENSP00000300061.2:n.1177-760T>C
NM_001039.3:c.1177-760T>C NP_001030.2:n.1177-760T>C
NM_001039.4:c.1177-760T>C MANE Select NP_001030.2:n.1177-760T>C