Canonical Allele Identifier: CA8154021
Gene: TAT HGNC NCBI

Linked Data

ClinVar Variation Id: 255935
ClinVar RCV Id: RCV000247319 RCV000273867 RCV001668427
dbSNP Id: rs78302875
ExAC: 16:71609856 C / T
gnomAD v2: 16-71609856-C-T
gnomAD v3: 16-71575953-C-T
gnomAD v4: 16-71575953-C-T
MyVariant Identifiers: chr16:g.71609856C>T (hg19) chr16:g.71575953C>T (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.71575953C>T , CM000678.2:g.71575953C>T GRCh38
NC_000016.9:g.71609856C>T , CM000678.1:g.71609856C>T GRCh37
NC_000016.8:g.70167357C>T NCBI36
NG_008235.1:g.6143G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355962.5:c.309G>A MANE Select ENSP00000348234.4:p.Ser103=
ENST00000355962.4:c.309G>A ENSP00000348234.4:p.Ser103=
ENST00000566010.1:n.559G>A
ENST00000566094.5:n.405G>A
NM_000353.2:c.309G>A NP_000344.1:p.Ser103=
NM_000353.3:c.309G>A MANE Select NP_000344.1:p.Ser103=
Search 100 bp 5'
Search 100 bp 3'