Canonical Allele Identifier: CA1955410133
Gene: TPH1 HGNC NCBI

Linked Data

dbSNP Id: rs1848015658

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18033737A>G , CM000673.2:g.18033737A>G GRCh38
NC_000011.9:g.18055284A>G , CM000673.1:g.18055284A>G GRCh37
NC_000011.8:g.18011860A>G NCBI36
NG_011947.1:g.12052T>C
NG_011947.2:g.12052T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.302-363T>C MANE Select ENSP00000508368.1:n.302-363T>C
ENST00000250018.6:c.302-363T>C ENSP00000250018.2:n.302-363T>C
ENST00000417164.5:c.302-363T>C ENSP00000403831.1:n.302-363T>C
ENST00000528338.1:c.332-363T>C ENSP00000436081.1:n.332-363T>C
NM_004179.2:c.302-363T>C NP_004170.1:n.302-363T>C
NM_004179.3:c.302-363T>C MANE Select NP_004170.1:n.302-363T>C