Canonical Allele Identifier: CA413437198
Gene: EFNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829887G>C , CM000685.2:g.68829887G>C GRCh38
NC_000023.10:g.68049730G>C , CM000685.1:g.68049730G>C GRCh37
NC_000023.9:g.67966455G>C NCBI36
NG_008887.1:g.5891G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000204961.5:c.111G>C MANE Select ENSP00000204961.4:p.Trp37Cys
ENST00000204961.4:c.111G>C ENSP00000204961.4:p.Trp37Cys
NM_004429.4:c.111G>C NP_004420.1:p.Trp37Cys
NM_004429.5:c.111G>C MANE Select NP_004420.1:p.Trp37Cys