Canonical Allele Identifier: CA411351503

Gene: MB

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35610910G>A , CM000684.2:g.35610910G>A	GRCh38
NC_000022.10:g.36006957G>A , CM000684.1:g.36006957G>A	GRCh37
NC_000022.9:g.34336903G>A	NCBI36
NG_007075.1:g.17445C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005368.3:c.292C>T MANE Select	NP_005359.1:p.His98Tyr
ENST00000397326.7:c.292C>T MANE Select	ENSP00000380489.2:p.His98Tyr
NM_001362846.1:c.292C>T	NP_001349775.1:p.His98Tyr
NM_001362846.2:c.292C>T	NP_001349775.1:p.His98Tyr
NM_001382809.1:c.292C>T	NP_001369738.1:p.His98Tyr
NM_001382810.1:c.292C>T	NP_001369739.1:p.His98Tyr
NM_001382811.1:c.292C>T	NP_001369740.1:p.His98Tyr
NM_001382812.1:c.127C>T	NP_001369741.1:p.His43Tyr
NM_001382813.1:c.127C>T	NP_001369742.1:p.His43Tyr
NM_005368.2:c.292C>T	NP_005359.1:p.His98Tyr
NM_203377.1:c.292C>T	NP_976311.1:p.His98Tyr
NM_203378.1:c.292C>T	NP_976312.1:p.His98Tyr
ENST00000359787.5:c.292C>T	ENSP00000352835.1:p.His98Tyr
ENST00000397326.6:c.292C>T	ENSP00000380489.2:p.His98Tyr
ENST00000397328.5:c.292C>T	ENSP00000380491.1:p.His98Tyr
ENST00000401702.5:c.127C>T	ENSP00000386060.1:p.His43Tyr
ENST00000406324.5:c.292C>T	ENSP00000384239.1:p.His98Tyr
ENST00000442617.1:c.127C>T	ENSP00000413309.1:p.His43Tyr
ENST00000443033.5:c.292C>T	ENSP00000403351.1:p.His98Tyr
ENST00000447607.5:c.292C>T	ENSP00000389263.1:p.His98Tyr
ENST00000451685.5:c.292C>T	ENSP00000397944.1:p.His98Tyr
XM_005261605.2:c.292C>T	XP_005261662.1:p.His98Tyr