Canonical Allele Identifier: CA569138424

Gene: BEND3

Linked Data

• dbSNP Id: rs1298171746
• gnomAD v2: 6-107400368-T-C
• gnomAD v3: 6-107079164-T-C
• gnomAD v4: 6-107079164-T-C
• MyVariant Identifiers: chr6:g.107400368T>C (hg19) ; chr6:g.107079164T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107079164T>C , CM000668.2:g.107079164T>C	GRCh38
NC_000006.11:g.107400368T>C , CM000668.1:g.107400368T>C	GRCh37
NC_000006.10:g.107507061T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369042.6:c.241-8214A>G MANE Select	ENSP00000358038.1:n.241-8214A>G
ENST00000369042.5:c.241-8214A>G	ENSP00000358038.1:n.241-8214A>G
ENST00000429433.3:c.241-8214A>G	ENSP00000411268.2:n.241-8214A>G
NM_001080450.2:c.241-8214A>G	NP_001073919.1:n.241-8214A>G
XM_005267079.2:c.241-8214A>G	XP_005267136.1:n.241-8214A>G
XM_005267080.2:c.241-8214A>G	XP_005267137.1:n.241-8214A>G
XM_011536005.1:c.241-8214A>G	XP_011534307.1:n.241-8214A>G
XM_011536006.1:c.241-8214A>G	XP_011534308.1:n.241-8214A>G
XM_011536007.1:c.241-8214A>G	XP_011534309.1:n.241-8214A>G
XM_005267079.4:c.241-8214A>G	XP_005267136.1:n.241-8214A>G
XM_005267080.4:c.241-8214A>G	XP_005267137.1:n.241-8214A>G
XM_011536005.3:c.241-8214A>G	XP_011534307.1:n.241-8214A>G
NM_001367314.1:c.241-8214A>G MANE Select	NP_001354243.1:n.241-8214A>G
NM_001080450.3:c.241-8214A>G	NP_001073919.1:n.241-8214A>G