Canonical Allele Identifier: CA1066074702

Gene: BANK1

Linked Data

• dbSNP Id: rs1725899918
• gnomAD v3: 4-101815981-T-C
• gnomAD v4: 4-101815981-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101815981T>C , CM000666.2:g.101815981T>C	GRCh38
NC_000004.11:g.102737138T>C , CM000666.1:g.102737138T>C	GRCh37
NC_000004.10:g.102956161T>C	NCBI36
NG_015824.1:g.30375T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-13827T>C MANE Select	ENSP00000320509.4:n.71-13827T>C
ENST00000322953.8:c.71-13827T>C	ENSP00000320509.4:n.71-13827T>C
ENST00000428908.5:c.70+25031T>C	ENSP00000412748.1:n.70+25031T>C
ENST00000444316.2:c.-21+2043T>C	ENSP00000388817.2:n.-21+2043T>C
ENST00000504592.5:c.26-13827T>C	ENSP00000421443.1:n.26-13827T>C
ENST00000508653.5:c.70+25031T>C	ENSP00000422314.1:n.70+25031T>C
NM_001083907.2:c.-21+2043T>C	NP_001077376.2:n.-21+2043T>C
NM_001127507.2:c.70+25031T>C	NP_001120979.2:n.70+25031T>C
NM_017935.4:c.71-13827T>C	NP_060405.4:n.71-13827T>C
XM_017008337.2:c.-20-13827T>C	XP_016863826.1:n.-20-13827T>C
NM_017935.5:c.71-13827T>C MANE Select	NP_060405.5:n.71-13827T>C
NM_001083907.3:c.-21+2043T>C	NP_001077376.3:n.-21+2043T>C
NM_001127507.3:c.70+25031T>C	NP_001120979.3:n.70+25031T>C