Canonical Allele Identifier: CA413437195
Gene: EFNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829886G>C , CM000685.2:g.68829886G>C GRCh38
NC_000023.10:g.68049729G>C , CM000685.1:g.68049729G>C GRCh37
NC_000023.9:g.67966454G>C NCBI36
NG_008887.1:g.5890G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000204961.5:c.110G>C MANE Select ENSP00000204961.4:p.Trp37Ser
ENST00000204961.4:c.110G>C ENSP00000204961.4:p.Trp37Ser
NM_004429.4:c.110G>C NP_004420.1:p.Trp37Ser
NM_004429.5:c.110G>C MANE Select NP_004420.1:p.Trp37Ser