Canonical Allele Identifier: CA2695234401
Gene: EFNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829682T>C , CM000685.2:g.68829682T>C GRCh38
NC_000023.10:g.68049525T>C , CM000685.1:g.68049525T>C GRCh37
NC_000023.9:g.67966250T>C NCBI36
NG_008887.1:g.5686T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.-95T>C MANE Select ENSP00000204961.4:n.-95T>C
ENST00000204961.4:c.-95T>C ENSP00000204961.4:n.-95T>C
NM_004429.4:c.-95T>C NP_004420.1:n.-95T>C
NM_004429.5:c.-95T>C MANE Select NP_004420.1:n.-95T>C