Canonical Allele Identifier: CA2693969569
Gene: EFNB1 HGNC NCBI

Linked Data

gnomAD v4: X-68829710-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829710G>T , CM000685.2:g.68829710G>T GRCh38
NC_000023.10:g.68049553G>T , CM000685.1:g.68049553G>T GRCh37
NC_000023.9:g.67966278G>T NCBI36
NG_008887.1:g.5714G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.-67G>T MANE Select ENSP00000204961.4:n.-67G>T
ENST00000204961.4:c.-67G>T ENSP00000204961.4:n.-67G>T
NM_004429.4:c.-67G>T NP_004420.1:n.-67G>T
NM_004429.5:c.-67G>T MANE Select NP_004420.1:n.-67G>T