Canonical Allele Identifier: CA413437206
Gene: EFNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.68049733C>A (hg19) chrX:g.68829890C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829890C>A , CM000685.2:g.68829890C>A GRCh38
NC_000023.10:g.68049733C>A , CM000685.1:g.68049733C>A GRCh37
NC_000023.9:g.67966458C>A NCBI36
NG_008887.1:g.5894C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.114C>A MANE Select ENSP00000204961.4:p.Ser38Arg
ENST00000204961.4:c.114C>A ENSP00000204961.4:p.Ser38Arg
NM_004429.4:c.114C>A NP_004420.1:p.Ser38Arg
NM_004429.5:c.114C>A MANE Select NP_004420.1:p.Ser38Arg
Search 100 bp 5'
Search 100 bp 3'