Canonical Allele Identifier: CA218516557
Gene: TPH1 HGNC NCBI

Linked Data

dbSNP Id: rs554363398
MyVariant Identifiers: chr11:g.18055160G>T (hg19) chr11:g.18033613G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18033613G>T , CM000673.2:g.18033613G>T GRCh38
NC_000011.9:g.18055160G>T , CM000673.1:g.18055160G>T GRCh37
NC_000011.8:g.18011736G>T NCBI36
NG_011947.1:g.12176C>A
NG_011947.2:g.12176C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.302-239C>A MANE Select ENSP00000508368.1:n.302-239C>A
ENST00000250018.6:c.302-239C>A ENSP00000250018.2:n.302-239C>A
ENST00000417164.5:c.302-239C>A ENSP00000403831.1:n.302-239C>A
ENST00000528338.1:c.332-239C>A ENSP00000436081.1:n.332-239C>A
NM_004179.2:c.302-239C>A NP_004170.1:n.302-239C>A
NM_004179.3:c.302-239C>A MANE Select NP_004170.1:n.302-239C>A
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