Canonical Allele Identifier: CA413438010
Gene: EFNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.68059563A>C (hg19) chrX:g.68839720A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68839720A>C , CM000685.2:g.68839720A>C GRCh38
NC_000023.10:g.68059563A>C , CM000685.1:g.68059563A>C GRCh37
NC_000023.9:g.67976288A>C NCBI36
NG_008887.1:g.15724A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.463A>C MANE Select ENSP00000204961.4:p.Thr155Pro
ENST00000204961.4:c.463A>C ENSP00000204961.4:p.Thr155Pro
NM_004429.4:c.463A>C NP_004420.1:p.Thr155Pro
NM_004429.5:c.463A>C MANE Select NP_004420.1:p.Thr155Pro
Search 100 bp 5'
Search 100 bp 3'