Canonical Allele Identifier: CA103073376

Gene: BANK1

Linked Data

• dbSNP Id: rs1017393110
• gnomAD v3: 4-101944048-G-C
• gnomAD v4: 4-101944048-G-C
• MyVariant Identifiers: chr4:g.102865205G>C (hg19) ; chr4:g.101944048G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101944048G>C , CM000666.2:g.101944048G>C	GRCh38
NC_000004.11:g.102865205G>C , CM000666.1:g.102865205G>C	GRCh37
NC_000004.10:g.103084228G>C	NCBI36
NG_015824.1:g.158442G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1206+25859G>C MANE Select	ENSP00000320509.4:n.1206+25859G>C
ENST00000322953.8:c.1206+25859G>C	ENSP00000320509.4:n.1206+25859G>C
ENST00000428908.5:c.807+25859G>C	ENSP00000412748.1:n.807+25859G>C
ENST00000444316.2:c.1116+25859G>C	ENSP00000388817.2:n.1116+25859G>C
ENST00000504592.5:c.1161+25859G>C	ENSP00000421443.1:n.1161+25859G>C
ENST00000508653.5:c.807+25859G>C	ENSP00000422314.1:n.807+25859G>C
NM_001083907.2:c.1116+25859G>C	NP_001077376.2:n.1116+25859G>C
NM_001127507.2:c.807+25859G>C	NP_001120979.2:n.807+25859G>C
NM_017935.4:c.1206+25859G>C	NP_060405.4:n.1206+25859G>C
XM_017008337.2:c.1116+25859G>C	XP_016863826.1:n.1116+25859G>C
NM_017935.5:c.1206+25859G>C MANE Select	NP_060405.5:n.1206+25859G>C
NM_001083907.3:c.1116+25859G>C	NP_001077376.3:n.1116+25859G>C
NM_001127507.3:c.807+25859G>C	NP_001120979.3:n.807+25859G>C