Canonical Allele Identifier: CA2435560652
Gene: EFNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829885T= , CM000685.2:g.68829885T= GRCh38
NC_000023.10:g.68049728T= , CM000685.1:g.68049728T= GRCh37
NC_000023.9:g.67966453T= NCBI36
NG_008887.1:g.5889T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.109T= MANE Select ENSP00000204961.4:p.Trp37=
ENST00000204961.4:c.109T= ENSP00000204961.4:p.Trp37=
NM_004429.4:c.109T= NP_004420.1:p.Trp37=
NM_004429.5:c.109T= MANE Select NP_004420.1:p.Trp37=