Canonical Allele Identifier: CA2260368418
Gene: HCRT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184509G= , CM000679.2:g.42184509G= GRCh38
NC_000017.10:g.40336527G= , CM000679.1:g.40336527G= GRCh37
NC_000017.9:g.37590053G= NCBI36
NG_011448.1:g.5944C=

Transcript Alleles

HGVS Amino-acid change
ENST00000293330.1:c.41C= MANE Select ENSP00000293330.1:p.Thr14=
NM_001524.1:c.41C= MANE Select NP_001515.1:p.Thr14=
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Search 100 bp 3'