Canonical Allele Identifier: CA395103547
Gene: SCNN1G HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.23226566A>G (hg19) chr16:g.23215245A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23215245A>G , CM000678.2:g.23215245A>G GRCh38
NC_000016.9:g.23226566A>G , CM000678.1:g.23226566A>G GRCh37
NC_000016.8:g.23134067A>G NCBI36
NG_011909.1:g.37527A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.1726A>G MANE Select ENSP00000300061.2:p.Lys576Glu
ENST00000300061.2:c.1726A>G ENSP00000300061.2:p.Lys576Glu
NM_001039.3:c.1726A>G NP_001030.2:p.Lys576Glu
NM_001039.4:c.1726A>G MANE Select NP_001030.2:p.Lys576Glu
Search 100 bp 5'
Search 100 bp 3'