Canonical Allele Identifier: CA2649007607
Gene: TBX19 HGNC NCBI

Linked Data

gnomAD v4: 1-168293366-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293366G>A , CM000663.2:g.168293366G>A GRCh38
NC_000001.10:g.168262604G>A , CM000663.1:g.168262604G>A GRCh37
NC_000001.9:g.166529228G>A NCBI36
NG_008244.1:g.17327G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+88G>A MANE Select ENSP00000356795.3:n.603+88G>A
ENST00000367821.7:c.603+88G>A ENSP00000356795.3:n.603+88G>A
ENST00000431969.5:c.400+88G>A
NM_005149.2:c.603+88G>A NP_005140.1:n.603+88G>A
NM_005149.3:c.603+88G>A MANE Select NP_005140.1:n.603+88G>A
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