Canonical Allele Identifier: CA2693969619
Gene: EFNB1 HGNC NCBI

Linked Data

gnomAD v4: X-68829772-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829772G>T , CM000685.2:g.68829772G>T GRCh38
NC_000023.10:g.68049615G>T , CM000685.1:g.68049615G>T GRCh37
NC_000023.9:g.67966340G>T NCBI36
NG_008887.1:g.5776G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.-5G>T MANE Select ENSP00000204961.4:n.-5G>T
ENST00000204961.4:c.-5G>T ENSP00000204961.4:n.-5G>T
NM_004429.4:c.-5G>T NP_004420.1:n.-5G>T
NM_004429.5:c.-5G>T MANE Select NP_004420.1:n.-5G>T