Canonical Allele Identifier: CA370807793
Gene: CHRNA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.27320526G>C (hg19) chr8:g.27463009G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27463009G>C , CM000670.2:g.27463009G>C GRCh38
NC_000008.10:g.27320526G>C , CM000670.1:g.27320526G>C GRCh37
NC_000008.9:g.27376443G>C NCBI36
NG_015827.1:g.21288C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000407991.3:c.1434C>G MANE Select ENSP00000385026.1:p.Asp478Glu
ENST00000240132.7:c.1389C>G ENSP00000240132.2:p.Asp463Glu
ENST00000407991.2:c.1434C>G ENSP00000385026.1:p.Asp478Glu
ENST00000520600.1:n.290-1255C>G
ENST00000520933.7:c.1368C>G ENSP00000429616.2:p.Asp456Glu
ENST00000523695.5:c.*836C>G ENSP00000430612.1:n.*836C>G
NM_000742.3:c.1434C>G NP_000733.2:p.Asp478Glu
NM_001282455.1:c.1389C>G NP_001269384.1:p.Asp463Glu
XM_005273397.1:c.957C>G XP_005273454.1:p.Asp319Glu
XM_006716282.1:c.1434C>G XP_006716345.1:p.Asp478Glu
XM_011544388.1:c.1434C>G XP_011542690.1:p.Asp478Glu
XM_011544389.1:c.840C>G XP_011542691.1:p.Asp280Glu
NM_001347705.1:c.957C>G NP_001334634.1:p.Asp319Glu
NM_001347706.1:c.957C>G NP_001334635.1:p.Asp319Glu
NM_001347707.1:c.840C>G NP_001334636.1:p.Asp280Glu
NM_001347708.1:c.840C>G NP_001334637.1:p.Asp280Glu
XM_011544389.2:c.840C>G XP_011542691.1:p.Asp280Glu
NM_000742.4:c.1434C>G MANE Select NP_000733.2:p.Asp478Glu
NM_001282455.2:c.1389C>G NP_001269384.1:p.Asp463Glu
NM_001347705.2:c.957C>G NP_001334634.1:p.Asp319Glu
NM_001347706.2:c.957C>G NP_001334635.1:p.Asp319Glu
NM_001347707.2:c.840C>G NP_001334636.1:p.Asp280Glu
NM_001347708.2:c.840C>G NP_001334637.1:p.Asp280Glu
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