Canonical Allele Identifier: CA683909166

Gene: TBX5

Linked Data

• dbSNP Id: rs1214631359
• MyVariant Identifiers: chr12:g.114792105C>G (hg19) ; chr12:g.114354300C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114354300C>G , CM000674.2:g.114354300C>G	GRCh38
NC_000012.11:g.114792105C>G , CM000674.1:g.114792105C>G	GRCh37
NC_000012.10:g.113276488C>G	NCBI36
NG_007373.1:g.59143G>C , LRG_670:g.59143G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.*1232G>C MANE Select	ENSP00000384152.3:n.*1232G>C
ENST00000310346.8:c.*1232G>C	ENSP00000309913.4:n.*1232G>C
ENST00000349716.9:c.*1232G>C	ENSP00000337723.5:n.*1232G>C
NM_000192.3:c.*1232G>C , LRG_670t1:c.*1232G>C	NP_000183.2:n.*1232G>C
NM_080717.2:c.*1232G>C	NP_542448.1:n.*1232G>C
NM_181486.2:c.*1232G>C	NP_852259.1:n.*1232G>C
XM_017019912.1:c.*1232G>C	XP_016875401.1:n.*1232G>C
NM_080717.3:c.*1232G>C	NP_542448.1:n.*1232G>C
NM_181486.4:c.*1232G>C MANE Select	NP_852259.1:n.*1232G>C
NM_080717.4:c.*1232G>C	NP_542448.1:n.*1232G>C