Canonical Allele Identifier: CA413437203

Gene: EFNB1

Linked Data

• MyVariant Identifiers: chrX:g.68049732G>A (hg19) ; chrX:g.68829889G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.68829889G>A , CM000685.2:g.68829889G>A	GRCh38
NC_000023.10:g.68049732G>A , CM000685.1:g.68049732G>A	GRCh37
NC_000023.9:g.67966457G>A	NCBI36
NG_008887.1:g.5893G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000204961.5:c.113G>A MANE Select	ENSP00000204961.4:p.Ser38Asn
ENST00000204961.4:c.113G>A	ENSP00000204961.4:p.Ser38Asn
NM_004429.4:c.113G>A	NP_004420.1:p.Ser38Asn
NM_004429.5:c.113G>A MANE Select	NP_004420.1:p.Ser38Asn