Canonical Allele Identifier: CA516988552
Gene: EFNB1 HGNC NCBI

Linked Data

gnomAD v4: X-68829842-C-T
MyVariant Identifiers: chrX:g.68049685C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829842C>T , CM000685.2:g.68829842C>T GRCh38
NC_000023.10:g.68049685C>T , CM000685.1:g.68049685C>T GRCh37
NC_000023.9:g.67966410C>T NCBI36
NG_008887.1:g.5846C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.66C>T MANE Select ENSP00000204961.4:p.Cys22=
ENST00000204961.4:c.66C>T ENSP00000204961.4:p.Cys22=
NM_004429.4:c.66C>T NP_004420.1:p.Cys22=
NM_004429.5:c.66C>T MANE Select NP_004420.1:p.Cys22=
Search 100 bp 5'
Search 100 bp 3'