Canonical Allele Identifier: CA2632290400
Gene: SCNN1G HGNC NCBI

Linked Data

gnomAD v4: 16-23196648-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23196648A>C , CM000678.2:g.23196648A>C GRCh38
NC_000016.9:g.23207969A>C , CM000678.1:g.23207969A>C GRCh37
NC_000016.8:g.23115470A>C NCBI36
NG_011909.1:g.18930A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.914-616A>C MANE Select ENSP00000300061.2:n.914-616A>C
ENST00000300061.2:c.914-616A>C ENSP00000300061.2:n.914-616A>C
NM_001039.3:c.914-616A>C NP_001030.2:n.914-616A>C
NM_001039.4:c.914-616A>C MANE Select NP_001030.2:n.914-616A>C
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