Canonical Allele Identifier: CA2331698854
Gene: TSHZ3 HGNC NCBI

Linked Data

dbSNP Id: rs1078373
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.31310224G>T , CM000681.2:g.31310224G>T GRCh38
NC_000019.9:g.31801130G>T , CM000681.1:g.31801130G>T GRCh37
NC_000019.8:g.36492970G>T NCBI36
NG_051203.1:g.44302C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000240587.5:c.41-30472C>A MANE Select ENSP00000240587.4:n.41-30472C>A
ENST00000651361.1:n.63+38956C>A
ENST00000240587.4:c.41-30472C>A ENSP00000240587.4:n.41-30472C>A
ENST00000558569.1:c.41-1515C>A ENSP00000475613.1:n.41-1515C>A
NM_020856.2:c.41-30472C>A NP_065907.2:n.41-30472C>A
NM_020856.3:c.41-30472C>A NP_065907.2:n.41-30472C>A
NR_138034.1:n.347-1515C>A
NR_138035.1:n.346+38956C>A
NR_138036.1:n.346+38956C>A
NM_020856.4:c.41-30472C>A MANE Select NP_065907.2:n.41-30472C>A
NR_138034.2:n.258-1515C>A
NR_138035.2:n.257+38956C>A
NR_138036.2:n.257+38956C>A
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