Canonical Allele Identifier: CA413438004
Gene: EFNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.68059560C>A (hg19) chrX:g.68839717C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68839717C>A , CM000685.2:g.68839717C>A GRCh38
NC_000023.10:g.68059560C>A , CM000685.1:g.68059560C>A GRCh37
NC_000023.9:g.67976285C>A NCBI36
NG_008887.1:g.15721C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.460C>A MANE Select ENSP00000204961.4:p.Arg154Ser
ENST00000204961.4:c.460C>A ENSP00000204961.4:p.Arg154Ser
NM_004429.4:c.460C>A NP_004420.1:p.Arg154Ser
NM_004429.5:c.460C>A MANE Select NP_004420.1:p.Arg154Ser
Search 100 bp 5'
Search 100 bp 3'