Canonical Allele Identifier: CA2693969559
Gene: EFNB1 HGNC NCBI

Linked Data

gnomAD v4: X-68829698-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829698C>A , CM000685.2:g.68829698C>A GRCh38
NC_000023.10:g.68049541C>A , CM000685.1:g.68049541C>A GRCh37
NC_000023.9:g.67966266C>A NCBI36
NG_008887.1:g.5702C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.-79C>A MANE Select ENSP00000204961.4:n.-79C>A
ENST00000204961.4:c.-79C>A ENSP00000204961.4:n.-79C>A
NM_004429.4:c.-79C>A NP_004420.1:n.-79C>A
NM_004429.5:c.-79C>A MANE Select NP_004420.1:n.-79C>A
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