Canonical Allele Identifier: CA1481082858
Gene: BANK1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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