Canonical Allele Identifier: CA597678479
Gene: TPH1 HGNC NCBI

Linked Data

dbSNP Id: rs1165758033

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18033689G>A , CM000673.2:g.18033689G>A GRCh38
NC_000011.9:g.18055236G>A , CM000673.1:g.18055236G>A GRCh37
NC_000011.8:g.18011812G>A NCBI36
NG_011947.1:g.12100C>T
NG_011947.2:g.12100C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.302-315C>T MANE Select ENSP00000508368.1:n.302-315C>T
ENST00000250018.6:c.302-315C>T ENSP00000250018.2:n.302-315C>T
ENST00000417164.5:c.302-315C>T ENSP00000403831.1:n.302-315C>T
ENST00000528338.1:c.332-315C>T ENSP00000436081.1:n.332-315C>T
NM_004179.2:c.302-315C>T NP_004170.1:n.302-315C>T
NM_004179.3:c.302-315C>T MANE Select NP_004170.1:n.302-315C>T