Canonical Allele Identifier: CA2736441994
Gene: THBD HGNC NCBI

Linked Data

dbSNP Id: rs1217892820
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23046216C>A , CM000682.2:g.23046216C>A GRCh38
NC_000020.10:g.23026853C>A , CM000682.1:g.23026853C>A GRCh37
NC_000020.9:g.22974853C>A NCBI36
NG_012027.1:g.8449G>T , LRG_168:g.8449G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377103.3:c.*1561G>T MANE Select ENSP00000366307.2:n.*1561G>T
ENST00000377103.2:c.*1561G>T ENSP00000366307.2:n.*1561G>T
NM_000361.2:c.*1561G>T , LRG_168t1:c.*1561G>T NP_000352.1:n.*1561G>T
NM_000361.3:c.*1561G>T MANE Select NP_000352.1:n.*1561G>T
Search 100 bp 5'
Search 100 bp 3'