Canonical Allele Identifier: CA4763269
Gene: TTPA HGNC NCBI

Linked Data

ClinVar Variation Id: 911009
ClinVar RCV Id: RCV001163238
dbSNP Id: rs371592549
ExAC: 8:63985479 T / C
gnomAD v2: 8-63985479-T-C
gnomAD v3: 8-63072920-T-C
gnomAD v4: 8-63072920-T-C
MyVariant Identifiers: chr8:g.63985479T>C (hg19) chr8:g.63072920T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072920T>C , CM000670.2:g.63072920T>C GRCh38
NC_000008.10:g.63985479T>C , CM000670.1:g.63985479T>C GRCh37
NC_000008.9:g.64148033T>C NCBI36
NG_016123.1:g.18134A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.358+15A>G MANE Select ENSP00000260116.4:n.358+15A>G
ENST00000260116.4:c.358+15A>G ENSP00000260116.4:n.358+15A>G
ENST00000521138.1:n.232+12898A>G
NM_000370.3:c.358+15A>G MANE Select NP_000361.1:n.358+15A>G
XM_006716468.2:c.205-8604A>G XP_006716531.1:n.205-8604A>G
XM_006716468.4:c.205-8604A>G XP_006716531.1:n.205-8604A>G
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