Canonical Allele Identifier: CA10664605
Gene: EPHB2 HGNC NCBI

Linked Data

dbSNP Id: rs4263970
gnomAD v2: 1-23063930-T-C
gnomAD v3: 1-22737437-T-C
gnomAD v4: 1-22737437-T-C
MyVariant Identifiers: chr1:g.23063930T>C (hg19) chr1:g.22737437T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22737437T>C , CM000663.2:g.22737437T>C GRCh38
NC_000001.10:g.23063930T>C , CM000663.1:g.23063930T>C GRCh37
NC_000001.9:g.22936517T>C NCBI36
NG_011804.2:g.31600T>C , LRG_780:g.31600T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374630.8:c.61+26394T>C MANE Select ENSP00000363761.3:n.61+26394T>C
ENST00000374630.7:c.61+26394T>C ENSP00000363761.3:n.61+26394T>C
ENST00000374632.7:c.61+26394T>C ENSP00000363763.3:n.61+26394T>C
ENST00000400191.7:c.61+26394T>C ENSP00000383053.3:n.61+26394T>C
ENST00000544305.5:c.61+26394T>C ENSP00000444174.1:n.61+26394T>C
NM_001309192.1:c.61+26394T>C NP_001296121.1:n.61+26394T>C
NM_001309193.1:c.61+26394T>C NP_001296122.1:n.61+26394T>C
NM_004442.6:c.61+26394T>C NP_004433.2:n.61+26394T>C
NM_004442.7:c.61+26394T>C , LRG_780t1:c.61+26394T>C NP_004433.2:n.61+26394T>C
NM_017449.3:c.61+26394T>C NP_059145.2:n.61+26394T>C
NM_017449.4:c.61+26394T>C , LRG_780t2:c.61+26394T>C NP_059145.2:n.61+26394T>C
XM_006710442.2:c.61+26394T>C XP_006710505.1:n.61+26394T>C
XM_006710442.4:c.61+26394T>C XP_006710505.1:n.61+26394T>C
NM_001309192.2:c.61+26394T>C NP_001296121.1:n.61+26394T>C
NM_001309193.2:c.61+26394T>C NP_001296122.1:n.61+26394T>C
NM_017449.5:c.61+26394T>C MANE Select NP_059145.2:n.61+26394T>C
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