Canonical Allele Identifier: CA516988518
Gene: EFNB1 HGNC NCBI

Linked Data

gnomAD v4: X-68829791-G-T
MyVariant Identifiers: chrX:g.68049634G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829791G>T , CM000685.2:g.68829791G>T GRCh38
NC_000023.10:g.68049634G>T , CM000685.1:g.68049634G>T GRCh37
NC_000023.9:g.67966359G>T NCBI36
NG_008887.1:g.5795G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000204961.5:c.15G>T MANE Select ENSP00000204961.4:p.Gly5=
ENST00000204961.4:c.15G>T ENSP00000204961.4:p.Gly5=
NM_004429.4:c.15G>T NP_004420.1:p.Gly5=
NM_004429.5:c.15G>T MANE Select NP_004420.1:p.Gly5=