Canonical Allele Identifier: CA510161054
Gene: THBD HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.23029917C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049280C>A , CM000682.2:g.23049280C>A GRCh38
NC_000020.10:g.23029917C>A , CM000682.1:g.23029917C>A GRCh37
NC_000020.9:g.22977917C>A NCBI36
NG_012027.1:g.5385G>T , LRG_168:g.5385G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377103.3:c.225G>T MANE Select ENSP00000366307.2:p.Leu75=
ENST00000377103.2:c.225G>T ENSP00000366307.2:p.Leu75=
NM_000361.2:c.225G>T , LRG_168t1:c.225G>T NP_000352.1:p.Leu75=
NM_000361.3:c.225G>T MANE Select NP_000352.1:p.Leu75=
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