Canonical Allele Identifier: CA2649007422
Gene: TBX19 HGNC NCBI

Linked Data

gnomAD v4: 1-168293018-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293018T>G , CM000663.2:g.168293018T>G GRCh38
NC_000001.10:g.168262256T>G , CM000663.1:g.168262256T>G GRCh37
NC_000001.9:g.166528880T>G NCBI36
NG_008244.1:g.16979T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.469-126T>G MANE Select ENSP00000356795.3:n.469-126T>G
ENST00000367821.7:c.469-126T>G ENSP00000356795.3:n.469-126T>G
ENST00000431969.5:c.266-126T>G
NM_005149.2:c.469-126T>G NP_005140.1:n.469-126T>G
NM_005149.3:c.469-126T>G MANE Select NP_005140.1:n.469-126T>G
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