Canonical Allele Identifier: CA11421711
Gene: EPHB1 HGNC NCBI

Linked Data

dbSNP Id: rs6766459

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.135197201G>T , CM000665.2:g.135197201G>T GRCh38
NC_000003.11:g.134916043G>T , CM000665.1:g.134916043G>T GRCh37
NC_000003.10:g.136398733G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398015.8:c.2131-4273G>T MANE Select ENSP00000381097.3:n.2131-4273G>T
ENST00000647596.1:c.2131-4273G>T ENSP00000497153.1:n.2131-4273G>T
ENST00000398015.7:c.2131-4273G>T ENSP00000381097.3:n.2131-4273G>T
ENST00000493838.1:c.814-4273G>T ENSP00000419574.1:n.814-4273G>T
NM_004441.4:c.2131-4273G>T NP_004432.1:n.2131-4273G>T
XM_011512540.1:c.2113-4273G>T XP_011510842.1:n.2113-4273G>T
XM_011512541.1:c.2065-4273G>T XP_011510843.1:n.2065-4273G>T
XM_011512542.1:c.361-4273G>T XP_011510844.1:n.361-4273G>T
XM_017005866.2:c.2293-4273G>T XP_016861355.1:n.2293-4273G>T
XM_017005867.1:c.2275-4273G>T XP_016861356.1:n.2275-4273G>T
XM_024453389.1:c.2227-4273G>T XP_024309157.1:n.2227-4273G>T
XM_024453390.1:c.2227-4273G>T XP_024309158.1:n.2227-4273G>T
NM_004441.5:c.2131-4273G>T MANE Select NP_004432.1:n.2131-4273G>T