Canonical Allele Identifier: CA1653702557
Gene: BEND3 HGNC NCBI

Linked Data

dbSNP Id: rs1627804

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107079224C>G , CM000668.2:g.107079224C>G GRCh38
NC_000006.11:g.107400428C>G , CM000668.1:g.107400428C>G GRCh37
NC_000006.10:g.107507121C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369042.6:c.241-8274G>C MANE Select ENSP00000358038.1:n.241-8274G>C
ENST00000369042.5:c.241-8274G>C ENSP00000358038.1:n.241-8274G>C
ENST00000429433.3:c.241-8274G>C ENSP00000411268.2:n.241-8274G>C
NM_001080450.2:c.241-8274G>C NP_001073919.1:n.241-8274G>C
XM_005267079.2:c.241-8274G>C XP_005267136.1:n.241-8274G>C
XM_005267080.2:c.241-8274G>C XP_005267137.1:n.241-8274G>C
XM_011536005.1:c.241-8274G>C XP_011534307.1:n.241-8274G>C
XM_011536006.1:c.241-8274G>C XP_011534308.1:n.241-8274G>C
XM_011536007.1:c.241-8274G>C XP_011534309.1:n.241-8274G>C
XM_005267079.4:c.241-8274G>C XP_005267136.1:n.241-8274G>C
XM_005267080.4:c.241-8274G>C XP_005267137.1:n.241-8274G>C
XM_011536005.3:c.241-8274G>C XP_011534307.1:n.241-8274G>C
NM_001367314.1:c.241-8274G>C MANE Select NP_001354243.1:n.241-8274G>C
NM_001080450.3:c.241-8274G>C NP_001073919.1:n.241-8274G>C