Canonical Allele Identifier: CA2693969561
Gene: EFNB1 HGNC NCBI

Linked Data

gnomAD v4: X-68829701-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829701C>A , CM000685.2:g.68829701C>A GRCh38
NC_000023.10:g.68049544C>A , CM000685.1:g.68049544C>A GRCh37
NC_000023.9:g.67966269C>A NCBI36
NG_008887.1:g.5705C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000204961.5:c.-76C>A MANE Select ENSP00000204961.4:n.-76C>A
ENST00000204961.4:c.-76C>A ENSP00000204961.4:n.-76C>A
NM_004429.4:c.-76C>A NP_004420.1:n.-76C>A
NM_004429.5:c.-76C>A MANE Select NP_004420.1:n.-76C>A
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