Canonical Allele Identifier: CA1955410119
Gene: TPH1 HGNC NCBI

Linked Data

dbSNP Id: rs1848015386

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18033688A>C , CM000673.2:g.18033688A>C GRCh38
NC_000011.9:g.18055235A>C , CM000673.1:g.18055235A>C GRCh37
NC_000011.8:g.18011811A>C NCBI36
NG_011947.1:g.12101T>G
NG_011947.2:g.12101T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.302-314T>G MANE Select ENSP00000508368.1:n.302-314T>G
ENST00000250018.6:c.302-314T>G ENSP00000250018.2:n.302-314T>G
ENST00000417164.5:c.302-314T>G ENSP00000403831.1:n.302-314T>G
ENST00000528338.1:c.332-314T>G ENSP00000436081.1:n.332-314T>G
NM_004179.2:c.302-314T>G NP_004170.1:n.302-314T>G
NM_004179.3:c.302-314T>G MANE Select NP_004170.1:n.302-314T>G