Canonical Allele Identifier: CA2260368490
Gene: HCRT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184627A= , CM000679.2:g.42184627A= GRCh38
NC_000017.10:g.40336645A= , CM000679.1:g.40336645A= GRCh37
NC_000017.9:g.37590171A= NCBI36
NG_011448.1:g.5826T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293330.1:c.22-99T= MANE Select ENSP00000293330.1:n.22-99T=
NM_001524.1:c.22-99T= MANE Select NP_001515.1:n.22-99T=