Canonical Allele Identifier: CA1291431460
Gene: THSD7B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.137118225A= , CM000664.2:g.137118225A= GRCh38
NC_000002.11:g.137875795A= , CM000664.1:g.137875795A= GRCh37
NC_000002.10:g.137592265A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000409968.6:c.1369+2932A= MANE Select ENSP00000387145.1:n.1369+2932A=
ENST00000272643.7:c.1369+2932A= ENSP00000272643.4:n.1369+2932A=
ENST00000409968.5:c.1369+2932A= ENSP00000387145.1:n.1369+2932A=
ENST00000413152.3:c.1276+2932A= ENSP00000413841.3:n.1276+2932A=
NM_001080427.1:c.1276+2932A= NP_001073896.1:n.1276+2932A=
NM_001316349.1:c.1369+2932A= NP_001303278.1:n.1369+2932A=
NM_001316349.2:c.1369+2932A= MANE Select NP_001303278.1:n.1369+2932A=
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