Canonical Allele Identifier: CA2213276553
Community Standard Title: NC_000016.10:g.23301864G=
Gene: SCNN1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23301864G= , CM000678.2:g.23301864G= GRCh38
NC_000016.9:g.23313185G= , CM000678.1:g.23313185G= GRCh37
NC_000016.8:g.23220686G= NCBI36
NG_011908.1:g.4595G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000569789.1:n.178+18060G=
XM_017023525.1:c.49+18060G= XP_016879014.1:n.49+18060G=
XM_017023526.1:c.49+18060G= XP_016879015.1:n.49+18060G=