Canonical Allele Identifier: CA371333665
Gene: TTPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.63985502T>G (hg19) chr8:g.63072943T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072943T>G , CM000670.2:g.63072943T>G GRCh38
NC_000008.10:g.63985502T>G , CM000670.1:g.63985502T>G GRCh37
NC_000008.9:g.64148056T>G NCBI36
NG_016123.1:g.18111A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260116.5:c.350A>C MANE Select ENSP00000260116.4:p.Tyr117Ser
ENST00000260116.4:c.350A>C ENSP00000260116.4:p.Tyr117Ser
ENST00000521138.1:n.232+12875A>C
NM_000370.3:c.350A>C MANE Select NP_000361.1:p.Tyr117Ser
XM_006716468.2:c.205-8627A>C XP_006716531.1:n.205-8627A>C
XM_006716468.4:c.205-8627A>C XP_006716531.1:n.205-8627A>C
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