Canonical Allele Identifier: CA935568256
Gene: TPH1 HGNC NCBI

Linked Data

dbSNP Id: rs1848015727
gnomAD v3: 11-18033747-C-T
gnomAD v4: 11-18033747-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18033747C>T , CM000673.2:g.18033747C>T GRCh38
NC_000011.9:g.18055294C>T , CM000673.1:g.18055294C>T GRCh37
NC_000011.8:g.18011870C>T NCBI36
NG_011947.1:g.12042G>A
NG_011947.2:g.12042G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.302-373G>A MANE Select ENSP00000508368.1:n.302-373G>A
ENST00000250018.6:c.302-373G>A ENSP00000250018.2:n.302-373G>A
ENST00000417164.5:c.302-373G>A ENSP00000403831.1:n.302-373G>A
ENST00000528338.1:c.332-373G>A ENSP00000436081.1:n.332-373G>A
NM_004179.2:c.302-373G>A NP_004170.1:n.302-373G>A
NM_004179.3:c.302-373G>A MANE Select NP_004170.1:n.302-373G>A
Search 100 bp 5'
Search 100 bp 3'