LDH info

Canonical Allele Identifier: CA11695751
Gene: BANK1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10028805

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101816093G>A , CM000666.2:g.101816093G>A GRCh38
NC_000004.11:g.102737250G>A , CM000666.1:g.102737250G>A GRCh37
NC_000004.10:g.102956273G>A NCBI36
NG_015824.1:g.30487G>A

Transcript Alleles

HGVS Amino-acid change
NM_001083907.2:c.-21+2155G>A VV NP_001077376.2:p.=
NM_001127507.2:c.70+25143G>A VV NP_001120979.2:p.=
NM_017935.4:c.71-13715G>A VV NP_060405.4:p.=
XM_017008337.2:c.-20-13715G>A XP_016863826.1:p.=
NM_017935.5:c.71-13715G>A VV MANE Preferred NP_060405.5:p.=
ENST00000322953.8:c.71-13715G>A ENSP00000320509.4:p.=
ENST00000428908.5:c.70+25143G>A ENSP00000412748.1:p.=
ENST00000444316.2:c.-21+2155G>A ENSP00000388817.2:p.=
ENST00000504592.5:c.26-13715G>A ENSP00000421443.1:p.=
ENST00000508653.5:c.70+25143G>A ENSP00000422314.1:p.=