Canonical Allele Identifier: CA1955410097
Gene: TPH1 HGNC NCBI

Linked Data

dbSNP Id: rs1590265190
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18033608G>A , CM000673.2:g.18033608G>A GRCh38
NC_000011.9:g.18055155G>A , CM000673.1:g.18055155G>A GRCh37
NC_000011.8:g.18011731G>A NCBI36
NG_011947.1:g.12181C>T
NG_011947.2:g.12181C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.302-234C>T MANE Select ENSP00000508368.1:n.302-234C>T
ENST00000250018.6:c.302-234C>T ENSP00000250018.2:n.302-234C>T
ENST00000417164.5:c.302-234C>T ENSP00000403831.1:n.302-234C>T
ENST00000528338.1:c.332-234C>T ENSP00000436081.1:n.332-234C>T
NM_004179.2:c.302-234C>T NP_004170.1:n.302-234C>T
NM_004179.3:c.302-234C>T MANE Select NP_004170.1:n.302-234C>T
Search 100 bp 5'
Search 100 bp 3'