Canonical Allele Identifier: CA103073421

Gene: BANK1

Linked Data

• dbSNP Id: rs903219023
• MyVariant Identifiers: chr4:g.102865456A>T (hg19) ; chr4:g.101944299A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101944299A>T , CM000666.2:g.101944299A>T	GRCh38
NC_000004.11:g.102865456A>T , CM000666.1:g.102865456A>T	GRCh37
NC_000004.10:g.103084479A>T	NCBI36
NG_015824.1:g.158693A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1206+26110A>T MANE Select	ENSP00000320509.4:n.1206+26110A>T
ENST00000322953.8:c.1206+26110A>T	ENSP00000320509.4:n.1206+26110A>T
ENST00000428908.5:c.807+26110A>T	ENSP00000412748.1:n.807+26110A>T
ENST00000444316.2:c.1116+26110A>T	ENSP00000388817.2:n.1116+26110A>T
ENST00000504592.5:c.1161+26110A>T	ENSP00000421443.1:n.1161+26110A>T
ENST00000508653.5:c.807+26110A>T	ENSP00000422314.1:n.807+26110A>T
NM_001083907.2:c.1116+26110A>T	NP_001077376.2:n.1116+26110A>T
NM_001127507.2:c.807+26110A>T	NP_001120979.2:n.807+26110A>T
NM_017935.4:c.1206+26110A>T	NP_060405.4:n.1206+26110A>T
XM_017008337.2:c.1116+26110A>T	XP_016863826.1:n.1116+26110A>T
NM_017935.5:c.1206+26110A>T MANE Select	NP_060405.5:n.1206+26110A>T
NM_001083907.3:c.1116+26110A>T	NP_001077376.3:n.1116+26110A>T
NM_001127507.3:c.807+26110A>T	NP_001120979.3:n.807+26110A>T