Canonical Allele Identifier: CA2739713797
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049555A>C , CM000682.2:g.23049555A>C GRCh38
NC_000020.10:g.23030192A>C , CM000682.1:g.23030192A>C GRCh37
NC_000020.9:g.22978192A>C NCBI36
NG_012027.1:g.5110T>G , LRG_168:g.5110T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.-51T>G MANE Select ENSP00000366307.2:n.-51T>G
ENST00000377103.2:c.-51T>G ENSP00000366307.2:n.-51T>G
NM_000361.2:c.-51T>G , LRG_168t1:c.-51T>G NP_000352.1:n.-51T>G
NM_000361.3:c.-51T>G MANE Select NP_000352.1:n.-51T>G