Canonical Allele Identifier: CA2739713804
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049564T>G , CM000682.2:g.23049564T>G GRCh38
NC_000020.10:g.23030201T>G , CM000682.1:g.23030201T>G GRCh37
NC_000020.9:g.22978201T>G NCBI36
NG_012027.1:g.5101A>C , LRG_168:g.5101A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.-60A>C MANE Select ENSP00000366307.2:n.-60A>C
ENST00000377103.2:c.-60A>C ENSP00000366307.2:n.-60A>C
NM_000361.2:c.-60A>C , LRG_168t1:c.-60A>C NP_000352.1:n.-60A>C
NM_000361.3:c.-60A>C MANE Select NP_000352.1:n.-60A>C