Canonical Allele Identifier: CA2652141741
Gene: THBD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049561C>T , CM000682.2:g.23049561C>T GRCh38
NC_000020.10:g.23030198C>T , CM000682.1:g.23030198C>T GRCh37
NC_000020.9:g.22978198C>T NCBI36
NG_012027.1:g.5104G>A , LRG_168:g.5104G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.-57G>A MANE Select ENSP00000366307.2:n.-57G>A
ENST00000377103.2:c.-57G>A ENSP00000366307.2:n.-57G>A
NM_000361.2:c.-57G>A , LRG_168t1:c.-57G>A NP_000352.1:n.-57G>A
NM_000361.3:c.-57G>A MANE Select NP_000352.1:n.-57G>A