Canonical Allele Identifier: CA3024722
Gene: BANK1 HGNC NCBI

Linked Data

dbSNP Id: rs17266594

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101829765T>C , CM000666.2:g.101829765T>C GRCh38
NC_000004.11:g.102750922T>C , CM000666.1:g.102750922T>C GRCh37
NC_000004.10:g.102969945T>C NCBI36
NG_015824.1:g.44159T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000322953.9:c.71-43T>C MANE Select ENSP00000320509.4:p.=
ENST00000322953.8:c.71-43T>C ENSP00000320509.4:p.=
ENST00000428908.5:c.71-25270T>C ENSP00000412748.1:p.=
ENST00000444316.2:c.-20-43T>C ENSP00000388817.2:p.=
ENST00000504592.5:c.26-43T>C ENSP00000421443.1:p.=
ENST00000508653.5:c.71-25270T>C ENSP00000422314.1:p.=
NM_001083907.2:c.-20-43T>C NP_001077376.2:p.=
NM_001127507.2:c.71-25270T>C NP_001120979.2:p.=
NM_017935.4:c.71-43T>C NP_060405.4:p.=
XM_017008337.2:c.-20-43T>C XP_016863826.1:p.=
NM_017935.5:c.71-43T>C MANE Select NP_060405.5:p.=
NM_001083907.3:c.-20-43T>C NP_001077376.3:p.=
NM_001127507.3:c.71-25270T>C NP_001120979.3:p.=