Canonical Allele Identifier: CA516988565
Gene: EFNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.68049697A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829854A>T , CM000685.2:g.68829854A>T GRCh38
NC_000023.10:g.68049697A>T , CM000685.1:g.68049697A>T GRCh37
NC_000023.9:g.67966422A>T NCBI36
NG_008887.1:g.5858A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.78A>T MANE Select ENSP00000204961.4:p.Thr26=
ENST00000204961.4:c.78A>T ENSP00000204961.4:p.Thr26=
NM_004429.4:c.78A>T NP_004420.1:p.Thr26=
NM_004429.5:c.78A>T MANE Select NP_004420.1:p.Thr26=
Search 100 bp 5'
Search 100 bp 3'