Canonical Allele Identifier: CA413436990
Gene: EFNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829789G>C , CM000685.2:g.68829789G>C GRCh38
NC_000023.10:g.68049632G>C , CM000685.1:g.68049632G>C GRCh37
NC_000023.9:g.67966357G>C NCBI36
NG_008887.1:g.5793G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000204961.5:c.13G>C MANE Select ENSP00000204961.4:p.Gly5Arg
ENST00000204961.4:c.13G>C ENSP00000204961.4:p.Gly5Arg
NM_004429.4:c.13G>C NP_004420.1:p.Gly5Arg
NM_004429.5:c.13G>C MANE Select NP_004420.1:p.Gly5Arg