Canonical Allele Identifier: CA449823048
Gene: TNXB HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32050075A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32082298A>C , CM000668.2:g.32082298A>C GRCh38
NC_000006.11:g.32050075A>C , CM000668.1:g.32050075A>C GRCh37
NC_000006.10:g.32158053A>C NCBI36
NG_008337.2:g.32077T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644971.2:c.3474T>G MANE Select ENSP00000496448.1:p.Thr1158=
ENST00000647633.1:c.4215T>G ENSP00000497649.1:p.Thr1405=
ENST00000375244.7:c.3474T>G ENSP00000364393.3:p.Thr1158=
ENST00000613214.4:c.3735T>G ENSP00000480067.1:p.Thr1245=
NM_019105.6:c.3474T>G NP_061978.6:p.Thr1158=
NM_001365276.1:c.3474T>G NP_001352205.1:p.Thr1158=
NM_019105.7:c.3474T>G NP_061978.6:p.Thr1158=
NM_001365276.2:c.3474T>G MANE Select NP_001352205.1:p.Thr1158=
NM_019105.8:c.3474T>G NP_061978.6:p.Thr1158=
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