Canonical Allele Identifier: CA2260368495
Gene: HCRT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184630C= , CM000679.2:g.42184630C= GRCh38
NC_000017.10:g.40336648C= , CM000679.1:g.40336648C= GRCh37
NC_000017.9:g.37590174C= NCBI36
NG_011448.1:g.5823G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293330.1:c.22-102G= MANE Select ENSP00000293330.1:n.22-102G=
NM_001524.1:c.22-102G= MANE Select NP_001515.1:n.22-102G=