Canonical Allele Identifier: CA553722588

Gene: BANK1

Linked Data

• dbSNP Id: rs1374496051
• gnomAD v2: 4-102737277-C-G
• gnomAD v3: 4-101816120-C-G
• gnomAD v4: 4-101816120-C-G
• MyVariant Identifiers: chr4:g.102737277C>G (hg19) ; chr4:g.101816120C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101816120C>G , CM000666.2:g.101816120C>G	GRCh38
NC_000004.11:g.102737277C>G , CM000666.1:g.102737277C>G	GRCh37
NC_000004.10:g.102956300C>G	NCBI36
NG_015824.1:g.30514C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.71-13688C>G MANE Select	ENSP00000320509.4:n.71-13688C>G
ENST00000322953.8:c.71-13688C>G	ENSP00000320509.4:n.71-13688C>G
ENST00000428908.5:c.70+25170C>G	ENSP00000412748.1:n.70+25170C>G
ENST00000444316.2:c.-21+2182C>G	ENSP00000388817.2:n.-21+2182C>G
ENST00000504592.5:c.26-13688C>G	ENSP00000421443.1:n.26-13688C>G
ENST00000508653.5:c.70+25170C>G	ENSP00000422314.1:n.70+25170C>G
NM_001083907.2:c.-21+2182C>G	NP_001077376.2:n.-21+2182C>G
NM_001127507.2:c.70+25170C>G	NP_001120979.2:n.70+25170C>G
NM_017935.4:c.71-13688C>G	NP_060405.4:n.71-13688C>G
XM_017008337.2:c.-20-13688C>G	XP_016863826.1:n.-20-13688C>G
NM_017935.5:c.71-13688C>G MANE Select	NP_060405.5:n.71-13688C>G
NM_001083907.3:c.-21+2182C>G	NP_001077376.3:n.-21+2182C>G
NM_001127507.3:c.70+25170C>G	NP_001120979.3:n.70+25170C>G