Canonical Allele Identifier: CA413438007
Gene: EFNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1710646
ClinVar RCV Id: RCV002291933
MyVariant Identifiers: chrX:g.68059561G>C (hg19) chrX:g.68839718G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68839718G>C , CM000685.2:g.68839718G>C GRCh38
NC_000023.10:g.68059561G>C , CM000685.1:g.68059561G>C GRCh37
NC_000023.9:g.67976286G>C NCBI36
NG_008887.1:g.15722G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.461G>C MANE Select ENSP00000204961.4:p.Arg154Pro
ENST00000204961.4:c.461G>C ENSP00000204961.4:p.Arg154Pro
NM_004429.4:c.461G>C NP_004420.1:p.Arg154Pro
NM_004429.5:c.461G>C MANE Select NP_004420.1:p.Arg154Pro
Search 100 bp 5'
Search 100 bp 3'