Canonical Allele Identifier: CA2577278041
Gene: CHRNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539878G>T , CM000664.2:g.232539878G>T GRCh38
NC_000002.11:g.233404588G>T , CM000664.1:g.233404588G>T GRCh37
NC_000002.10:g.233112832G>T NCBI36
NG_012954.1:g.5152G>T
NG_012954.2:g.5187G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.55+76G>T MANE Select ENSP00000498757.1:n.55+76G>T
ENST00000389492.3:c.55+76G>T ENSP00000374143.3:n.55+76G>T
ENST00000389494.7:c.55+76G>T ENSP00000374145.3:n.55+76G>T
ENST00000485094.1:n.76+76G>T
NM_005199.4:c.55+76G>T NP_005190.4:n.55+76G>T
NM_005199.5:c.55+76G>T MANE Select NP_005190.4:n.55+76G>T