Canonical Allele Identifier: CA103070469

Gene: BANK1

Linked Data

• dbSNP Id: rs914508250
• gnomAD v3: 4-101918040-T-G
• gnomAD v4: 4-101918040-T-G
• MyVariant Identifiers: chr4:g.102839197T>G (hg19) ; chr4:g.101918040T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918040T>G , CM000666.2:g.101918040T>G	GRCh38
NC_000004.11:g.102839197T>G , CM000666.1:g.102839197T>G	GRCh37
NC_000004.10:g.103058220T>G	NCBI36
NG_015824.1:g.132434T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.1057T>G MANE Select	ENSP00000320509.4:p.Phe353Val
ENST00000322953.8:c.1057T>G	ENSP00000320509.4:p.Phe353Val
ENST00000428908.5:c.658T>G	ENSP00000412748.1:p.Phe220Val
ENST00000444316.2:c.967T>G	ENSP00000388817.2:p.Phe323Val
ENST00000504592.5:c.1012T>G	ENSP00000421443.1:p.Phe338Val
ENST00000508653.5:c.658T>G	ENSP00000422314.1:p.Phe220Val
NM_001083907.2:c.967T>G	NP_001077376.2:p.Phe323Val
NM_001127507.2:c.658T>G	NP_001120979.2:p.Phe220Val
NM_017935.4:c.1057T>G	NP_060405.4:p.Phe353Val
XM_017008337.2:c.967T>G	XP_016863826.1:p.Phe323Val
NM_017935.5:c.1057T>G MANE Select	NP_060405.5:p.Phe353Val
NM_001083907.3:c.967T>G	NP_001077376.3:p.Phe323Val
NM_001127507.3:c.658T>G	NP_001120979.3:p.Phe220Val