Canonical Allele Identifier: CA8154097

Gene: TAT

Linked Data

• ClinVar Variation Id: 320415
• ClinVar RCV Id: RCV000325241 ; RCV001683288
• dbSNP Id: rs74344827
• ExAC: 16:71610276 G / A
• gnomAD v2: 16-71610276-G-A
• gnomAD v3: 16-71576373-G-A
• gnomAD v4: 16-71576373-G-A
• MyVariant Identifiers: chr16:g.71610276G>A (hg19) ; chr16:g.71576373G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.71576373G>A , CM000678.2:g.71576373G>A	GRCh38
NC_000016.9:g.71610276G>A , CM000678.1:g.71610276G>A	GRCh37
NC_000016.8:g.70167777G>A	NCBI36
NG_008235.1:g.5723C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355962.5:c.43C>T MANE Select	ENSP00000348234.4:p.Pro15Ser
ENST00000355962.4:c.43C>T	ENSP00000348234.4:p.Pro15Ser
ENST00000566010.1:n.139C>T
ENST00000566094.5:n.139C>T
NM_000353.2:c.43C>T	NP_000344.1:p.Pro15Ser
NM_000353.3:c.43C>T MANE Select	NP_000344.1:p.Pro15Ser