Canonical Allele Identifier: CA31493199
Gene: TBX19 HGNC NCBI

Linked Data

dbSNP Id: rs536784923
gnomAD v3: 1-168293081-C-T
gnomAD v4: 1-168293081-C-T
MyVariant Identifiers: chr1:g.168262319C>T (hg19) chr1:g.168293081C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293081C>T , CM000663.2:g.168293081C>T GRCh38
NC_000001.10:g.168262319C>T , CM000663.1:g.168262319C>T GRCh37
NC_000001.9:g.166528943C>T NCBI36
NG_008244.1:g.17042C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.469-63C>T MANE Select ENSP00000356795.3:n.469-63C>T
ENST00000367821.7:c.469-63C>T ENSP00000356795.3:n.469-63C>T
ENST00000431969.5:c.266-63C>T
NM_005149.2:c.469-63C>T NP_005140.1:n.469-63C>T
NM_005149.3:c.469-63C>T MANE Select NP_005140.1:n.469-63C>T
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Search 100 bp 3'