Canonical Allele Identifier: CA2619886830
Gene: TPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938876G>T , CM000674.2:g.71938876G>T GRCh38
NC_000012.11:g.72332656G>T , CM000674.1:g.72332656G>T GRCh37
NC_000012.10:g.70618923G>T NCBI36
NG_008279.1:g.5031G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.-111G>T MANE Select ENSP00000329093.3:n.-111G>T
ENST00000333850.3:c.-111G>T ENSP00000329093.3:n.-111G>T
NM_173353.3:c.-111G>T NP_775489.2:n.-111G>T
NM_173353.4:c.-111G>T MANE Select NP_775489.2:n.-111G>T