Canonical Allele Identifier: CA977622395
Gene: GNAO1 HGNC NCBI

Linked Data

dbSNP Id: rs1650514909

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56354804C>T , CM000678.2:g.56354804C>T GRCh38
NC_000016.9:g.56388716C>T , CM000678.1:g.56388716C>T GRCh37
NC_000016.8:g.54946217C>T NCBI36
NG_042800.1:g.168466C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262493.12:c.878-62C>T MANE Select ENSP00000262493.6:n.878-62C>T
ENST00000562316.6:c.545-1299C>T ENSP00000457238.2:n.545-1299C>T
ENST00000564727.2:c.182-62C>T ENSP00000454971.2:n.182-62C>T
ENST00000568375.2:c.116-62C>T
ENST00000638185.1:n.1093-62C>T
ENST00000638210.1:n.1178-62C>T
ENST00000638705.1:c.878-62C>T ENSP00000491223.1:n.878-62C>T
ENST00000638836.1:n.788-62C>T
ENST00000639055.1:n.1599-62C>T
ENST00000639251.1:n.779-62C>T
ENST00000639268.1:c.513-62C>T
ENST00000639341.1:c.403-62C>T
ENST00000639770.1:c.916-62C>T ENSP00000491999.1:n.916-62C>T
ENST00000640390.1:n.808-62C>T
ENST00000640469.1:c.242-62C>T ENSP00000491875.1:n.242-62C>T
ENST00000640560.1:n.654-62C>T
ENST00000640893.1:c.*276-62C>T ENSP00000492677.1:n.*276-62C>T
ENST00000262493.10:c.878-62C>T ENSP00000262493.6:n.878-62C>T
ENST00000564727.1:c.98-62C>T ENSP00000454971.1:n.98-62C>T
ENST00000568375.1:n.116-62C>T
NM_020988.2:c.878-62C>T NP_066268.1:n.878-62C>T
XM_011523003.1:c.752-62C>T XP_011521305.1:n.752-62C>T
XM_011523003.3:c.752-62C>T XP_011521305.1:n.752-62C>T
NM_020988.3:c.878-62C>T MANE Select NP_066268.1:n.878-62C>T