Canonical Allele Identifier: CA719198833
Gene: SCNN1G HGNC NCBI

Linked Data

dbSNP Id: rs1259712408
gnomAD v3: 16-23211493-A-G
gnomAD v4: 16-23211493-A-G
MyVariant Identifiers: chr16:g.23222814A>G (hg19) chr16:g.23211493A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23211493A>G , CM000678.2:g.23211493A>G GRCh38
NC_000016.9:g.23222814A>G , CM000678.1:g.23222814A>G GRCh37
NC_000016.8:g.23130315A>G NCBI36
NG_011909.1:g.33775A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300061.3:c.1177-541A>G MANE Select ENSP00000300061.2:n.1177-541A>G
ENST00000300061.2:c.1177-541A>G ENSP00000300061.2:n.1177-541A>G
NM_001039.3:c.1177-541A>G NP_001030.2:n.1177-541A>G
NM_001039.4:c.1177-541A>G MANE Select NP_001030.2:n.1177-541A>G
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