Canonical Allele Identifier: CA388453132

Gene: EDNRB

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77918517G>T , CM000675.2:g.77918517G>T	GRCh38
NC_000013.10:g.78492652G>T , CM000675.1:g.78492652G>T	GRCh37
NC_000013.9:g.77390653G>T	NCBI36
NG_011630.2:g.62013C>A
NG_011630.3:g.61207C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001122659.3:c.57C>A MANE Select	NP_001116131.1:p.Cys19Ter
ENST00000646607.2:c.57C>A MANE Select	ENSP00000493527.1:p.Cys19Ter
NM_000115.3:c.57C>A	NP_000106.1:p.Cys19Ter
NM_000115.4:c.57C>A	NP_000106.1:p.Cys19Ter
NM_000115.5:c.57C>A	NP_000106.1:p.Cys19Ter
NM_001122659.2:c.57C>A	NP_001116131.1:p.Cys19Ter
NM_001201397.1:c.327C>A	NP_001188326.1:p.Cys109Ter
NM_003991.3:c.57C>A	NP_003982.1:p.Cys19Ter
NM_003991.4:c.57C>A	NP_003982.1:p.Cys19Ter
ENST00000334286.7:c.57C>A	ENSP00000335311.5:p.Cys19Ter
ENST00000377211.8:c.327C>A	ENSP00000366416.4:p.Cys109Ter
ENST00000475537.1:c.57C>A	ENSP00000487082.1:p.Cys19Ter
ENST00000475537.2:c.57C>A	ENSP00000487082.2:p.Cys19Ter
ENST00000626030.1:c.57C>A	ENSP00000486202.1:p.Cys19Ter
ENST00000643890.1:c.57C>A	ENSP00000495815.1:p.Cys19Ter
ENST00000646605.1:c.57C>A	ENSP00000494278.1:p.Cys19Ter
ENST00000646948.1:c.57C>A	ENSP00000493895.1:p.Cys19Ter
XM_005266275.2:c.57C>A	XP_005266332.2:p.Cys19Ter
XM_011534949.1:c.57C>A	XP_011533251.1:p.Cys19Ter