Canonical Allele Identifier: CA784465740

Gene: BANK1

Linked Data

• dbSNP Id: rs4522865
• MyVariant Identifiers: chr4:g.102715888G>T (hg19) ; chr4:g.101794731G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101794731G>T , CM000666.2:g.101794731G>T	GRCh38
NC_000004.11:g.102715888G>T , CM000666.1:g.102715888G>T	GRCh37
NC_000004.10:g.102934911G>T	NCBI36
NG_015824.1:g.9125G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.70+3781G>T MANE Select	ENSP00000320509.4:n.70+3781G>T
ENST00000322953.8:c.70+3781G>T	ENSP00000320509.4:n.70+3781G>T
ENST00000428908.5:c.70+3781G>T	ENSP00000412748.1:n.70+3781G>T
ENST00000504592.5:c.26-35077G>T	ENSP00000421443.1:n.26-35077G>T
ENST00000508653.5:c.70+3781G>T	ENSP00000422314.1:n.70+3781G>T
NM_001127507.2:c.70+3781G>T	NP_001120979.2:n.70+3781G>T
NM_017935.4:c.70+3781G>T	NP_060405.4:n.70+3781G>T
XM_017008337.2:c.-21+4159G>T	XP_016863826.1:n.-21+4159G>T
NM_017935.5:c.70+3781G>T MANE Select	NP_060405.5:n.70+3781G>T
NM_001127507.3:c.70+3781G>T	NP_001120979.3:n.70+3781G>T