Canonical Allele Identifier: CA1772813266
Gene: CHRNA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27463023G= , CM000670.2:g.27463023G= GRCh38
NC_000008.10:g.27320540G= , CM000670.1:g.27320540G= GRCh37
NC_000008.9:g.27376457G= NCBI36
NG_015827.1:g.21274C=

Transcript Alleles

HGVS Amino-acid change
ENST00000407991.3:c.1420C= MANE Select ENSP00000385026.1:p.His474=
ENST00000240132.7:c.1375C= ENSP00000240132.2:p.His459=
ENST00000407991.2:c.1420C= ENSP00000385026.1:p.His474=
ENST00000520600.1:n.290-1269C=
ENST00000520933.7:c.1354C= ENSP00000429616.2:p.His452=
ENST00000523695.5:c.*822C= ENSP00000430612.1:n.*822C=
NM_000742.3:c.1420C= NP_000733.2:p.His474=
NM_001282455.1:c.1375C= NP_001269384.1:p.His459=
XM_005273397.1:c.943C= XP_005273454.1:p.His315=
XM_006716282.1:c.1420C= XP_006716345.1:p.His474=
XM_011544388.1:c.1420C= XP_011542690.1:p.His474=
XM_011544389.1:c.826C= XP_011542691.1:p.His276=
NM_001347705.1:c.943C= NP_001334634.1:p.His315=
NM_001347706.1:c.943C= NP_001334635.1:p.His315=
NM_001347707.1:c.826C= NP_001334636.1:p.His276=
NM_001347708.1:c.826C= NP_001334637.1:p.His276=
XM_011544389.2:c.826C= XP_011542691.1:p.His276=
NM_000742.4:c.1420C= MANE Select NP_000733.2:p.His474=
NM_001282455.2:c.1375C= NP_001269384.1:p.His459=
NM_001347705.2:c.943C= NP_001334634.1:p.His315=
NM_001347706.2:c.943C= NP_001334635.1:p.His315=
NM_001347707.2:c.826C= NP_001334636.1:p.His276=
NM_001347708.2:c.826C= NP_001334637.1:p.His276=