Canonical Allele Identifier: CA2649007314
Gene: TBX19 HGNC NCBI

Linked Data

gnomAD v4: 1-168291114-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291114T>C , CM000663.2:g.168291114T>C GRCh38
NC_000001.10:g.168260352T>C , CM000663.1:g.168260352T>C GRCh37
NC_000001.9:g.166526976T>C NCBI36
NG_008244.1:g.15075T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.204-46T>C MANE Select ENSP00000356795.3:n.204-46T>C
ENST00000367821.7:c.204-46T>C ENSP00000356795.3:n.204-46T>C
NM_005149.2:c.204-46T>C NP_005140.1:n.204-46T>C
NM_005149.3:c.204-46T>C MANE Select NP_005140.1:n.204-46T>C
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