Canonical Allele Identifier: CA413437238

Gene: EFNB1

Linked Data

• MyVariant Identifiers: chrX:g.68049747A>G (hg19) ; chrX:g.68829904A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.68829904A>G , CM000685.2:g.68829904A>G	GRCh38
NC_000023.10:g.68049747A>G , CM000685.1:g.68049747A>G	GRCh37
NC_000023.9:g.67966472A>G	NCBI36
NG_008887.1:g.5908A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000204961.5:c.128A>G MANE Select	ENSP00000204961.4:p.Lys43Arg
ENST00000204961.4:c.128A>G	ENSP00000204961.4:p.Lys43Arg
NM_004429.4:c.128A>G	NP_004420.1:p.Lys43Arg
NM_004429.5:c.128A>G MANE Select	NP_004420.1:p.Lys43Arg