Canonical Allele Identifier: CA351006838
Gene: CHRNG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539998A>T , CM000664.2:g.232539998A>T GRCh38
NC_000002.11:g.233404708A>T , CM000664.1:g.233404708A>T GRCh37
NC_000002.10:g.233112952A>T NCBI36
NG_012954.1:g.5272A>T
NG_012954.2:g.5307A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.62A>T MANE Select ENSP00000498757.1:p.Gln21Leu
ENST00000389492.3:c.62A>T ENSP00000374143.3:p.Gln21Leu
ENST00000389494.7:c.62A>T ENSP00000374145.3:p.Gln21Leu
ENST00000485094.1:n.83A>T
NM_005199.4:c.62A>T NP_005190.4:p.Gln21Leu
NM_005199.5:c.62A>T MANE Select NP_005190.4:p.Gln21Leu