Canonical Allele Identifier: CA3024728

Gene: BANK1

Linked Data

• dbSNP Id: rs763534941
• ExAC: 4:102750976 G / T
• gnomAD v2: 4-102750976-G-T
• gnomAD v4: 4-101829819-G-T
• MyVariant Identifiers: chr4:g.102750976G>T (hg19) ; chr4:g.101829819G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829819G>T , CM000666.2:g.101829819G>T	GRCh38
NC_000004.11:g.102750976G>T , CM000666.1:g.102750976G>T	GRCh37
NC_000004.10:g.102969999G>T	NCBI36
NG_015824.1:g.44213G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.82G>T MANE Select	ENSP00000320509.4:p.Asp28Tyr
ENST00000322953.8:c.82G>T	ENSP00000320509.4:p.Asp28Tyr
ENST00000428908.5:c.71-25216G>T	ENSP00000412748.1:n.71-25216G>T
ENST00000444316.2:c.-9G>T	ENSP00000388817.2:n.-9G>T
ENST00000504592.5:c.37G>T	ENSP00000421443.1:p.Asp13Tyr
ENST00000508653.5:c.71-25216G>T	ENSP00000422314.1:n.71-25216G>T
NM_001083907.2:c.-9G>T	NP_001077376.2:n.-9G>T
NM_001127507.2:c.71-25216G>T	NP_001120979.2:n.71-25216G>T
NM_017935.4:c.82G>T	NP_060405.4:p.Asp28Tyr
XM_017008337.2:c.-9G>T	XP_016863826.1:n.-9G>T
NM_017935.5:c.82G>T MANE Select	NP_060405.5:p.Asp28Tyr
NM_001083907.3:c.-9G>T	NP_001077376.3:n.-9G>T
NM_001127507.3:c.71-25216G>T	NP_001120979.3:n.71-25216G>T