Canonical Allele Identifier: CA370809397
Gene: CHRNA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27463310A>T , CM000670.2:g.27463310A>T GRCh38
NC_000008.10:g.27320827A>T , CM000670.1:g.27320827A>T GRCh37
NC_000008.9:g.27376744A>T NCBI36
NG_015827.1:g.20987T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407991.3:c.1133T>A MANE Select ENSP00000385026.1:p.Leu378His
ENST00000240132.7:c.1088T>A ENSP00000240132.2:p.Leu363His
ENST00000407991.2:c.1133T>A ENSP00000385026.1:p.Leu378His
ENST00000520600.1:n.290-1556T>A
ENST00000520933.7:c.1067T>A ENSP00000429616.2:p.Leu356His
ENST00000523695.5:c.*535T>A ENSP00000430612.1:n.*535T>A
NM_000742.3:c.1133T>A NP_000733.2:p.Leu378His
NM_001282455.1:c.1088T>A NP_001269384.1:p.Leu363His
XM_005273397.1:c.656T>A XP_005273454.1:p.Leu219His
XM_006716282.1:c.1133T>A XP_006716345.1:p.Leu378His
XM_011544388.1:c.1133T>A XP_011542690.1:p.Leu378His
XM_011544389.1:c.539T>A XP_011542691.1:p.Leu180His
NM_001347705.1:c.656T>A NP_001334634.1:p.Leu219His
NM_001347706.1:c.656T>A NP_001334635.1:p.Leu219His
NM_001347707.1:c.539T>A NP_001334636.1:p.Leu180His
NM_001347708.1:c.539T>A NP_001334637.1:p.Leu180His
XM_011544389.2:c.539T>A XP_011542691.1:p.Leu180His
NM_000742.4:c.1133T>A MANE Select NP_000733.2:p.Leu378His
NM_001282455.2:c.1088T>A NP_001269384.1:p.Leu363His
NM_001347705.2:c.656T>A NP_001334634.1:p.Leu219His
NM_001347706.2:c.656T>A NP_001334635.1:p.Leu219His
NM_001347707.2:c.539T>A NP_001334636.1:p.Leu180His
NM_001347708.2:c.539T>A NP_001334637.1:p.Leu180His