Canonical Allele Identifier: CA719198878
Gene: SCNN1G HGNC NCBI

Linked Data

dbSNP Id: rs1243270243
MyVariant Identifiers: chr16:g.23222871C>T (hg19) chr16:g.23211550C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23211550C>T , CM000678.2:g.23211550C>T GRCh38
NC_000016.9:g.23222871C>T , CM000678.1:g.23222871C>T GRCh37
NC_000016.8:g.23130372C>T NCBI36
NG_011909.1:g.33832C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300061.3:c.1177-484C>T MANE Select ENSP00000300061.2:n.1177-484C>T
ENST00000300061.2:c.1177-484C>T ENSP00000300061.2:n.1177-484C>T
NM_001039.3:c.1177-484C>T NP_001030.2:n.1177-484C>T
NM_001039.4:c.1177-484C>T MANE Select NP_001030.2:n.1177-484C>T
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