Canonical Allele Identifier: CA2260368488
Gene: HCRT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184625C= , CM000679.2:g.42184625C= GRCh38
NC_000017.10:g.40336643C= , CM000679.1:g.40336643C= GRCh37
NC_000017.9:g.37590169C= NCBI36
NG_011448.1:g.5828G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293330.1:c.22-97G= MANE Select ENSP00000293330.1:n.22-97G=
NM_001524.1:c.22-97G= MANE Select NP_001515.1:n.22-97G=