Canonical Allele Identifier: CA2435564169
Gene: EFNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68839720A= , CM000685.2:g.68839720A= GRCh38
NC_000023.10:g.68059563A= , CM000685.1:g.68059563A= GRCh37
NC_000023.9:g.67976288A= NCBI36
NG_008887.1:g.15724A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.463A= MANE Select ENSP00000204961.4:p.Thr155=
ENST00000204961.4:c.463A= ENSP00000204961.4:p.Thr155=
NM_004429.4:c.463A= NP_004420.1:p.Thr155=
NM_004429.5:c.463A= MANE Select NP_004420.1:p.Thr155=