Canonical Allele Identifier: CA2581057589
Community Standard Title: NM_000869.6(HTR3A):c.-42T>G
Gene: HTR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113975284T>G , CM000673.2:g.113975284T>G GRCh38
NC_000011.9:g.113846006T>G , CM000673.1:g.113846006T>G GRCh37
NC_000011.8:g.113351216T>G NCBI36
NG_013058.1:g.5210T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000869.6:c.-42T>G MANE Select NP_000860.3:n.-42T>G
ENST00000504030.7:c.-42T>G MANE Select ENSP00000424189.2:n.-42T>G
NM_000869.5:c.-24T>G NP_000860.2:n.-24T>G
NM_213621.3:c.-24T>G NP_998786.2:n.-24T>G
NM_213621.4:c.-42T>G NP_998786.3:n.-42T>G
NR_046363.1:n.210T>G
NR_046363.2:n.177T>G
ENST00000355556.6:c.-24T>G ENSP00000347754.2:n.-24T>G
ENST00000375498.6:c.-24T>G ENSP00000364648.2:n.-24T>G
ENST00000504030.6:c.-42T>G ENSP00000424189.2:n.-42T>G
ENST00000506841.6:c.-42T>G ENSP00000424776.2:n.-42T>G