Canonical Allele Identifier: CA103070446

Gene: BANK1

Linked Data

• dbSNP Id: rs537418293
• MyVariant Identifiers: chr4:g.102838841G>C (hg19) ; chr4:g.101917684G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101917684G>C , CM000666.2:g.101917684G>C	GRCh38
NC_000004.11:g.102838841G>C , CM000666.1:g.102838841G>C	GRCh37
NC_000004.10:g.103057864G>C	NCBI36
NG_015824.1:g.132078G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1010-309G>C MANE Select	ENSP00000320509.4:n.1010-309G>C
ENST00000322953.8:c.1010-309G>C	ENSP00000320509.4:n.1010-309G>C
ENST00000428908.5:c.611-309G>C	ENSP00000412748.1:n.611-309G>C
ENST00000444316.2:c.920-309G>C	ENSP00000388817.2:n.920-309G>C
ENST00000504592.5:c.965-309G>C	ENSP00000421443.1:n.965-309G>C
ENST00000508653.5:c.611-309G>C	ENSP00000422314.1:n.611-309G>C
NM_001083907.2:c.920-309G>C	NP_001077376.2:n.920-309G>C
NM_001127507.2:c.611-309G>C	NP_001120979.2:n.611-309G>C
NM_017935.4:c.1010-309G>C	NP_060405.4:n.1010-309G>C
XM_017008337.2:c.920-309G>C	XP_016863826.1:n.920-309G>C
NM_017935.5:c.1010-309G>C MANE Select	NP_060405.5:n.1010-309G>C
NM_001083907.3:c.920-309G>C	NP_001077376.3:n.920-309G>C
NM_001127507.3:c.611-309G>C	NP_001120979.3:n.611-309G>C