Canonical Allele Identifier: CA2806257879

Gene: SCNN1G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23211271C>T , CM000678.2:g.23211271C>T	GRCh38
NC_000016.9:g.23222592C>T , CM000678.1:g.23222592C>T	GRCh37
NC_000016.8:g.23130093C>T	NCBI36
NG_011909.1:g.33553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300061.3:c.1177-763C>T MANE Select	ENSP00000300061.2:n.1177-763C>T
ENST00000300061.2:c.1177-763C>T	ENSP00000300061.2:n.1177-763C>T
NM_001039.3:c.1177-763C>T	NP_001030.2:n.1177-763C>T
NM_001039.4:c.1177-763C>T MANE Select	NP_001030.2:n.1177-763C>T