Canonical Allele Identifier: CA2579984143
Gene: EFNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2500937
ClinVar RCV Id: RCV003226122

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829877_68829890del , CM000685.2:g.68829877_68829890del GRCh38
NC_000023.10:g.68049720_68049733del , CM000685.1:g.68049720_68049733del GRCh37
NC_000023.9:g.67966445_67966458del NCBI36
NG_008887.1:g.5881_5894del

Transcript Alleles

HGVS Amino-acid change
ENST00000204961.5:c.101_114del MANE Select ENSP00000204961.4:p.Pro34LeufsTer?
ENST00000204961.4:c.101_114del ENSP00000204961.4:p.Pro34LeufsTer?
NM_004429.4:c.101_114del NP_004420.1:p.Pro34LeufsTer?
NM_004429.5:c.101_114del MANE Select NP_004420.1:p.Pro34LeufsTer?