Canonical Allele Identifier: CA2649007326
Gene: TBX19 HGNC NCBI

Linked Data

gnomAD v4: 1-168291152-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291152C>A , CM000663.2:g.168291152C>A GRCh38
NC_000001.10:g.168260390C>A , CM000663.1:g.168260390C>A GRCh37
NC_000001.9:g.166527014C>A NCBI36
NG_008244.1:g.15113C>A

Transcript Alleles

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