Canonical Allele Identifier: CA984262679
Gene: TBX21 HGNC NCBI

Linked Data

dbSNP Id: rs2032161690
gnomAD v3: 17-47733392-G-C
gnomAD v4: 17-47733392-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733392G>C , CM000679.2:g.47733392G>C GRCh38
NC_000017.10:g.45810758G>C , CM000679.1:g.45810758G>C GRCh37
NC_000017.9:g.43165757G>C NCBI36
NG_012166.1:g.5149G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.-63G>C MANE Select ENSP00000177694.1:n.-63G>C
ENST00000177694.1:c.-63G>C ENSP00000177694.1:n.-63G>C
NM_013351.1:c.-63G>C NP_037483.1:n.-63G>C
XM_011524698.1:c.-63G>C XP_011523000.1:n.-63G>C
NM_013351.2:c.-63G>C MANE Select NP_037483.1:n.-63G>C
Search 100 bp 5'
Search 100 bp 3'