Canonical Allele Identifier: CA413437064
Gene: EFNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.68049665A>T (hg19) chrX:g.68829822A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829822A>T , CM000685.2:g.68829822A>T GRCh38
NC_000023.10:g.68049665A>T , CM000685.1:g.68049665A>T GRCh37
NC_000023.9:g.67966390A>T NCBI36
NG_008887.1:g.5826A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.46A>T MANE Select ENSP00000204961.4:p.Met16Leu
ENST00000204961.4:c.46A>T ENSP00000204961.4:p.Met16Leu
NM_004429.4:c.46A>T NP_004420.1:p.Met16Leu
NM_004429.5:c.46A>T MANE Select NP_004420.1:p.Met16Leu
Search 100 bp 5'
Search 100 bp 3'