Canonical Allele Identifier: CA1205614336

Gene: TBX19

Linked Data

• dbSNP Id: rs1197711388

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293569C>T , CM000663.2:g.168293569C>T	GRCh38
NC_000001.10:g.168262807C>T , CM000663.1:g.168262807C>T	GRCh37
NC_000001.9:g.166529431C>T	NCBI36
NG_008244.1:g.17530C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.603+291C>T MANE Select	ENSP00000356795.3:n.603+291C>T
ENST00000367821.7:c.603+291C>T	ENSP00000356795.3:n.603+291C>T
ENST00000431969.5:c.400+291C>T
NM_005149.2:c.603+291C>T	NP_005140.1:n.603+291C>T
NM_005149.3:c.603+291C>T MANE Select	NP_005140.1:n.603+291C>T