Canonical Allele Identifier: CA553723079

Gene: BANK1

Linked Data

• dbSNP Id: rs1444707871
• gnomAD v2: 4-102740149-G-A
• gnomAD v3: 4-101818992-G-A
• gnomAD v4: 4-101818992-G-A
• MyVariant Identifiers: chr4:g.102740149G>A (hg19) ; chr4:g.101818992G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818992G>A , CM000666.2:g.101818992G>A	GRCh38
NC_000004.11:g.102740149G>A , CM000666.1:g.102740149G>A	GRCh37
NC_000004.10:g.102959172G>A	NCBI36
NG_015824.1:g.33386G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-10816G>A MANE Select	ENSP00000320509.4:n.71-10816G>A
ENST00000322953.8:c.71-10816G>A	ENSP00000320509.4:n.71-10816G>A
ENST00000428908.5:c.70+28042G>A	ENSP00000412748.1:n.70+28042G>A
ENST00000444316.2:c.-21+5054G>A	ENSP00000388817.2:n.-21+5054G>A
ENST00000504592.5:c.26-10816G>A	ENSP00000421443.1:n.26-10816G>A
ENST00000508653.5:c.70+28042G>A	ENSP00000422314.1:n.70+28042G>A
NM_001083907.2:c.-21+5054G>A	NP_001077376.2:n.-21+5054G>A
NM_001127507.2:c.70+28042G>A	NP_001120979.2:n.70+28042G>A
NM_017935.4:c.71-10816G>A	NP_060405.4:n.71-10816G>A
XM_017008337.2:c.-20-10816G>A	XP_016863826.1:n.-20-10816G>A
NM_017935.5:c.71-10816G>A MANE Select	NP_060405.5:n.71-10816G>A
NM_001083907.3:c.-21+5054G>A	NP_001077376.3:n.-21+5054G>A
NM_001127507.3:c.70+28042G>A	NP_001120979.3:n.70+28042G>A