Canonical Allele Identifier: CA395114733

Gene: SCNN1B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23353051G>C , CM000678.2:g.23353051G>C	GRCh38
NC_000016.9:g.23364372G>C , CM000678.1:g.23364372G>C	GRCh37
NC_000016.8:g.23271873G>C	NCBI36
NG_011908.1:g.55782G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000336.3:c.562G>C MANE Select	NP_000327.2:p.Gly188Arg
ENST00000343070.7:c.562G>C MANE Select	ENSP00000345751.2:p.Gly188Arg
NM_000336.2:c.562G>C	NP_000327.2:p.Gly188Arg
ENST00000307331.9:c.697G>C	ENSP00000302874.5:p.Gly233Arg
ENST00000343070.6:c.562G>C	ENSP00000345751.2:p.Gly188Arg
ENST00000564275.5:c.562G>C	ENSP00000457754.1:p.Gly188Arg
ENST00000566870.1:n.367G>C
ENST00000568085.5:c.562G>C	ENSP00000455673.1:p.Gly188Arg
ENST00000568923.5:c.562G>C	ENSP00000456309.1:p.Gly188Arg
XM_011545913.1:c.595G>C	XP_011544215.1:p.Gly199Arg
XM_011545913.2:c.595G>C	XP_011544215.1:p.Gly199Arg
XM_011545914.1:c.580G>C	XP_011544216.1:p.Gly194Arg
XM_017023525.1:c.619G>C	XP_016879014.1:p.Gly207Arg
XM_017023526.1:c.619G>C	XP_016879015.1:p.Gly207Arg